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Just now! Another key Philips product has completely exited the market
Medical Device Business Review 2025-03-04 14:36:39
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Philips spent 2.6 billion on the "first and only," which is completely exiting the market in less than 5 years!

01

Causing injuries to 20 people!

Another important device from Philips is completely exiting the market

A few hours ago, the FDA officially issued a notice that Philips is recalling its Tack endovascular system, with the recall level being the most severe, Class I, indicating that the product series may cause serious injury or death.

Due to serious safety concerns, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

Philips Spent 2.6 Billion on the "First and Only," Completely Exited the Market in Less Than 5 Years!

01

Causing Injuries to 20 People!

Another Important Philips Device Completely Exits the Market

A few hours ago, the FDA officially issued a notice that Philips is recalling its Tack Endovascular System, with the recall level being the most severe, Class I, indicating that the series of products may cause serious injury or death.

Due to serious safety hazards, this product will completely exit the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

Philips Spent 2.6 Billion on the "First and Only," Completely Exited the Market in Less Than 5 Years!

01

Caused Injuries to 20 People!

Another Important Philips Device Completely Exits the Market

A few hours ago, the FDA officially announced that Philips is recalling its Tack Endovascular System, with the recall level being the most severe, Level I, indicating that the product series may cause serious injury or death.

Due to serious safety hazards, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

Philips Spent 2.6 Billion on the "First and Only," and It's Completely Exited the Market in Less Than 5 Years!

01

Caused Injuries to 20 People!

Another Important Philips Device Completely Exits the Market

A few hours ago, the FDA officially announced that Philips is recalling its Tack Endovascular System, with the recall classified as the most serious level, indicating that the series of products may cause serious injury or death.

Due to serious safety hazards, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

Philips spent 2.6 billion on the "first and only," and it's completely exiting the market in less than 5 years!

01

Causing injuries to 20 people!

Another important Philips device is completely exiting the market

A few hours ago, the FDA officially issued a notice that Philips is recalling its Tack endovascular system, with the recall level being the most severe, Level I, indicating that the series of products may cause serious injury or death.

Due to serious safety hazards, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

Philips has spent 2.6 billion on the "first and only," but it completely exited the market in less than five years!

01

Causing injuries to 20 people!

Another important Philips device is completely exiting the market

A few hours ago, the FDA officially issued a notice that Philips is recalling its Tack Endovascular System, with the recall level being the most severe, Class I, indicating that the series of products may cause serious injury or death.

Due to serious safety hazards, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

Philips spent 2.6 billion to acquire the "first and only," which is completely exiting the market in less than 5 years!

01

Causing injuries to 20 people!

Another important device from Philips is completely exiting the market

A few hours ago, the FDA officially issued a notice that Philips is recalling its Tack Endovascular System, with the recall level being the most severe, Level I, indicating that the series of products may cause serious injury or death.

Due to serious safety hazards, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

Image source: FDA official website

Philips spent 2.6 billion to acquire the "first and only," but it completely exited the market in less than 5 years!

01

Causing injuries to 20 people!

Another important Philips device is completely exiting the market

A few hours ago, the FDA officially issued a notice that Philips is recalling its Tack endovascular system, with the recall level being the most severe, Class I, indicating that the series of products may cause serious injury or death.

Due to serious safety hazards, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

Image source: FDA official website

The official notice states that the use of the affectedSure, please provide the content that needs to be translated.

Philips Spent 2.6 Billion on the "First and Only," Exits the Market Completely in Less Than 5 Years!

01

Causing Injuries to 20 People!

Another Important Philips Device Exits the Market Completely

A few hours ago, the FDA officially announced that Philips is recalling its Tack Endovascular System, with the recall level being the most serious, Class I, which means the series of products may cause serious injury or death.

Due to serious safety hazards, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

Image Source: FDA Official Website

The official notice states that using the affected product may result in serious adverse health consequences, including short-term risks such as partial or complete obstructionSure, please provide the content that needs to be translated.

Philips Spent 2.6 Billion on the "First and Only," but It's Completely Exiting the Market in Less Than 5 Years!

01

Caused Injuries to 20 People!

Another Important Philips Device is Completely Exiting the Market

A few hours ago, the FDA officially announced that Philips is recalling its Tack Endovascular System, with the recall classified as the most serious Class I, meaning the product series may cause serious injury or death.

Due to serious safety concerns, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

Image Source: FDA Official Website

The official notice states that using the affected product may result in serious adverse health consequences, including short-term risks such as partial or complete blockage of blood flow (occlusion), holes or tears in the inner wall of the artery (dissection) and penetration through the entireSure, please provide the content that needs to be translated.

Philips Spent 2.6 Billion on the "First and Only," but It's Completely Exited the Market in Less Than 5 Years!

01

Causing Injuries to 20 People!

Another Important Philips Device is Completely Exiting the Market

A few hours ago, the FDA officially issued a notice that Philips is recalling its Tack Endovascular System, with the recall classified as the most severe level, meaning the series of products may cause serious injury or death.

Due to serious safety hazards, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

Image Source: FDA Official Website

The official notice states that using the affected product may result in serious adverse health consequences, including short-term risks such as partial or complete blockage of blood flow (occlusion), holes or tears in the inner wall of the artery (dissection) and penetration through the entire arterial wall (perforation); as well as long-term risks such as pain, tissue loss, expansion, or implantation of stents.Sure, please provide the content that needs to be translated.

Philips Spent 2.6 Billion on the "First and Only," and It's Completely Exited the Market in Less Than 5 Years!

01

Causing Injuries to 20 People!

Another Key Philips Device is Completely Exiting the Market

A few hours ago, the FDA officially announced that Philips is recalling its Tack Endovascular System, with the recall classified as the most serious, Level I, meaning the series of products may cause serious injury or death.

Due to serious safety concerns, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

Image Source: FDA Official Website

The official notice states that using the affected product may result in serious adverse health consequences, including short-term risks such as partial or complete blockage of blood flow (occlusion), holes or tears in the inner wall of the artery (dissection) and penetration through the entire arterial wall (perforation); and long-term risks such as pain, tissue loss, re-narrowing of the blood vessel where a stent was placed (restenosis), the need for bypass surgery, amputation, and death.Sure, please provide the content that needs to be translated.

Philips spent 2.6 billion on the "first and only," which completely exited the market in less than 5 years!

01

Causing injuries to 20 people!

Another important Philips device is completely exiting the market

A few hours ago, the FDA officially issued a notice that Philips is recalling its Tack Endovascular System, with the recall level being the most severe, Class I, meaning the series of products may cause serious injury or death.

Due to serious safety hazards, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

Image source: FDA official website

The official notice states that using the affected product may result in serious adverse health consequences, including short-term risks such as partial or complete blockage of blood flow (occlusion), holes or tears in the inner wall of the artery (dissection) and penetration through the entire arterial wall (perforation); and long-term risks such as pain, tissue loss, expansion or re-narrowing of the blood vessel where the stent was implanted (restenosis), the need for bypass surgery, amputation, and death, with 20 injuries already reported.

SpecificSure, please provide the content that needs to be translated.

Philips Spent 2.6 Billion on the "First and Only," and It's Completely Exiting the Market in Less Than 5 Years!

01

Causing Injuries to 20 People!

Another Important Philips Device is Completely Exiting the Market

A few hours ago, the FDA officially announced that Philips is recalling its Tack Endovascular System, with the recall classified as the most serious Class I, indicating that the series of products may cause serious injury or death.

Due to serious safety hazards, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

Image Source: FDA Official Website

The official notice states that using the affected products may result in serious adverse health consequences, including short-term risks such as partial or complete blockage of blood flow (occlusion), holes or tears in the inner wall of the artery (dissection) and penetration through the entire arterial wall (perforation); and long-term risks such as pain, tissue loss, expansion or narrowing of the blood vessel where a stent was implanted (restenosis), the need for bypass surgery, amputation, and death. Twenty people have already been reported injured.

Specific product information is as follows:

Philips spent 2.6 billion to buy the "first and only," but it completely exited the market in less than 5 years!

01

Causing injuries to 20 people!

Another important Philips device is completely exiting the market

A few hours ago, the FDA officially announced that Philips is recalling its Tack Endovascular System, with the recall classified as the most serious level, meaning the series of products may cause serious injury or death.

Due to serious safety hazards, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

Image source: FDA official website

The official notice states that using the affected product may result in serious adverse health consequences, including short-term risks such as partial or complete blockage of blood flow (occlusion), holes or tears in the inner wall of the artery (dissection) and penetration through the entire arterial wall (perforation); and long-term risks such as pain, tissue loss, re-narrowing of the vessel that has been expanded or had a stent implanted (restenosis), the need for bypass surgery, amputation, and death. Twenty injuries have already been reported.

Specific product information is as follows:

Philips Spent 2.6 Billion on the "First and Only," and It's Completely Exiting the Market in Less Than 5 Years!

01

Causing Injuries to 20 People!

Another Important Philips Device is Completely Exiting the Market

A few hours ago, the FDA officially issued a notice that Philips is recalling its Tack Endovascular System, with the recall level being the most severe, Class I, indicating that the series of products may cause serious injury or death.

Due to serious safety hazards, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

Image source: FDA official website

The official notice states that using the affected product may result in serious adverse health consequences, including short-term risks such as partial or complete blockage of blood flow (occlusion), holes or tears in the inner wall of the artery (dissection) and penetration through the entire arterial wall (perforation); and long-term risks such as pain, tissue loss, re-narrowing of the vessel where the stent was placed (restenosis), the need for bypass surgery, amputation, and death. Twenty injuries have already been reported.

Specific product information is as follows:

Sure, please provide the content that needs to be translated.

Philips Spent 2.6 Billion on the "First and Only," and It's Completely Exiting the Market in Less Than 5 Years!

01

Caused Injuries to 20 People!

Another Important Philips Device is Completely Exiting the Market

A few hours ago, the FDA officially announced that Philips is recalling its Tack Endovascular System, with the recall classified as the most serious, Class I, meaning the series of products could potentially cause serious injury or death.

Due to serious safety concerns, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

Image Source: FDA Official Website

The official notice states that using the affected product may result in serious adverse health consequences, including short-term risks such as partial or complete blockage of blood flow (occlusion), holes or tears in the inner wall of the artery (dissection) and penetration through the entire arterial wall (perforation); and long-term risks such as pain, tissue loss, re-narrowing of the vessel where a stent was placed (restenosis), the need for bypass surgery, amputation, and death. Twenty people have already been reported injured.

Specific product information is as follows:

Philips spent 2.6 billion to acquire the "first and only," but it completely exited the market in less than 5 years!

01

Causing injuries to 20 people!

Another important Philips device is completely exiting the market

A few hours ago, the FDA officially announced that Philips is recalling its Tack endovascular system, with the recall level being the most serious, Class I, indicating that the series of products may cause serious injury or death.

Due to serious safety concerns, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

Image source: FDA official website

The official notice states that using the affected product may result in serious adverse health consequences, including short-term risks such as partial or complete blockage of blood flow (occlusion), holes or tears in the inner wall of the artery (dissection) and penetration through the entire arterial wall (perforation); and long-term risks, such as pain, tissue loss, re-narrowing of the vessel where a stent was implanted (restenosis), the need for bypass surgery, amputation, and death. Twenty injuries have been reported so far.

Specific product information is as follows:

Recalled Product

Philips has spent 2.6 billion to buy the "first and only," but it is completely exiting the market in less than 5 years!

01

Causing injuries to 20 people!

Another important Philips device is completely exiting the market

A few hours ago, the FDA officially issued a notice that Philips is recalling its Tack endovascular system, with the recall level being the most serious, Class I, indicating that the series of products may cause serious injury or death.

Due to serious safety hazards, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

Image source: FDA official website

The official notice states that using the affected products may result in serious adverse health consequences, including short-term risks such as partial or complete blockage of blood flow (occlusion), holes or tears in the inner wall of the artery (dissection) and penetration through the entire arterial wall (perforation); and long-term risks such as pain, tissue loss, re-narrowing of the expanded or stented vessel (restenosis), the need for bypass surgery, amputation, and death, with 20 injuries already reported.

Specific product information is as follows:

Recalled product
Sure, please provide the content that needs to be translated.

Philips has spent 2.6 billion to buy the "first and only," but it completely exited the market in less than 5 years!

01

Causing injuries to 20 people!

Another important Philips device is completely exiting the market

A few hours ago, the FDA officially issued a notice that Philips is recalling its Tack endovascular system, with the recall level being the most severe, Level I, which means the series of products may cause serious injury or death.

Due to serious safety hazards, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

Image source: FDA official website

The official notice states that using the affected product may result in serious adverse health consequences, including short-term risks such as partial or complete blockage of blood flow (occlusion), holes or tears in the inner wall of the artery (dissection) and penetration through the entire arterial wall (perforation); and long-term risks such as pain, tissue loss, re-narrowing of the expanded or stented vessel (restenosis), the need for bypass surgery, amputation, and death. Twenty injuries have already been reported.

Specific product information is as follows:

Recalled Product

Philips spent 2.6 billion to acquire the "first and only," but it completely exited the market in less than 5 years!

01

Causing injuries to 20 people!

Another important Philips device is completely exiting the market

A few hours ago, the FDA officially issued a notice that Philips is recalling its Tack endovascular system, with the recall level being the most severe, Class I, indicating that the series of products may cause serious injury or death.

Due to serious safety hazards, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

Image source: FDA official website

The official notice states that the use of the affected product may result in serious adverse health consequences, including short-term risks such as partial or complete blockage of blood flow (occlusion), holes or tears in the inner wall of the artery (dissection) and penetration through the entire arterial wall (perforation); and long-term risks such as pain, tissue loss, expansion, or re-narrowing of the blood vessel where the stent was implanted (restenosis), the need for bypass surgery, amputation, and death. Twenty people have been reported injured.

Specific product information is as follows:

Recalled Product

Philips has spent 2.6 billion to buy the "first and only," but it is completely exiting the market in less than 5 years!

01

Causing injuries to 20 people!

Another important Philips device is completely exiting the market

A few hours ago, the FDA officially issued a notice that Philips is recalling its Tack Endovascular System, with the recall classified as the most serious level, indicating that the series of products may cause serious injury or death.

Due to serious safety hazards, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using and remove it.

image.png

Image source: FDA official website

The official notice states that using the affected products may result in serious adverse health consequences, including short-term risks such as partial or complete blockage of blood flow (occlusion), holes or tears in the inner wall of the artery (dissection) and penetration through the entire arterial wall (perforation); and long-term risks such as pain, tissue loss, re-narrowing of the vessel where the stent was implanted (restenosis), the need for bypass surgery, amputation, and death. Twenty injuries have been reported so far.

Specific product information is as follows:

Recalled Product

    Philips has spent 2.6 billion on the "first and only," but it is completely exiting the market in less than 5 years!

    01

    Caused 20 Injuries!

    Another Important Philips Device Completely Exits the Market

    A few hours ago, the FDA officially issued a notice that Philips is recalling its Tack Endovascular System, with the recall level being the most severe, Class I, indicating that the series of products may cause serious injury or death.

    Due to serious safety hazards, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

    image.png

    Image source: FDA official website

    The official notice states that using the affected products may result in serious adverse health consequences, including short-term risks such as partial or complete blockage of blood flow (occlusion), holes or tears in the inner wall of the artery (dissection) and penetration through the entire arterial wall (perforation); and long-term risks such as pain, tissue loss, re-narrowing of the vessel where a stent was placed (restenosis), the need for bypass surgery, amputation, and death. Twenty injuries have been reported so far.

    Specific product information is as follows:

    Recalled Product

Sure, please provide the content that needs to be translated.

Philips Spent 2.6 Billion on the "First and Only," and It's Completely Exited the Market in Less Than 5 Years!

01

Causing Injuries to 20 People!

Another Important Philips Device Completely Exits the Market

A few hours ago, the FDA officially issued a notice that Philips is recalling its Tack Endovascular System, with the recall classified as the most serious, Level I, indicating that the series of products may cause serious injury or death.

Due to serious safety concerns, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

Image Source: FDA Official Website

The official notification states that using the affected product may result in severe adverse health consequences, including short-term risks such as partial or complete blockage of blood flow (occlusion), holes or tears in the inner wall of the artery (dissection) and penetration through the entire arterial wall (perforation); and long-term risks such as pain, tissue loss, expansion or re-narrowing of the blood vessel where the stent is implanted (restenosis), the need for bypass surgery, amputation, and death. Twenty injuries have been reported so far.

Specific product information is as follows:

Recalled Product

    • Product Name: 

Sure, please provide the content that needs to be translated.

Philips has spent 2.6 billion to buy the "first and only," but it completely exited the market in less than 5 years!

01

Causing injuries to 20 people!

Another important Philips device is completely exiting the market

A few hours ago, the FDA officially announced that Philips is recalling its Tack endovascular system, with the recall classified as the most serious level, indicating that the series of products may cause serious injury or death.

Due to serious safety hazards, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

Image source: FDA official website

The official notice states that using the affected product may cause serious adverse health consequences, including short-term risks such as partial or complete blockage of blood flow (occlusion), holes or tears in the inner wall of the artery (dissection) and penetration through the entire arterial wall (perforation); and long-term risks such as pain, tissue loss, narrowing of the expanded or stented vessel (restenosis), the need for bypass surgery, amputation, and death, with 20 injuries already reported.

Specific product information is as follows:

Recalled Product

    • Product Name: 

Philips spent 2.6 billion to acquire the "first and only," but it completely exited the market in less than 5 years!

01

Causing Injuries to 20 People!

Another Important Philips Device Completely Exits the Market

A few hours ago, the FDA officially announced that Philips is recalling its Tack Endovascular System, with the recall classified as the most serious level, indicating that the series of products may cause serious injury or death.

Due to serious safety hazards, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

Image source: FDA official website

The official notice states that using the affected product may result in serious adverse health consequences, including short-term risks such as partial or complete blockage of blood flow (occlusion), holes or tears in the inner wall of the artery (dissection) and penetration through the entire arterial wall (perforation); and long-term risks such as pain, tissue loss, re-narrowing of the vessel where a stent was placed (restenosis), the need for bypass surgery, amputation, and death. Twenty injuries have already been reported.

Specific product information is as follows:

Recalled Product

    • Product Name: 

Philips spent 2.6 billion on the "first and only," but it completely exited the market in less than 5 years!

01

Caused 20 Injuries!

Another Important Philips Device Completely Exits the Market

A few hours ago, the FDA officially issued a notice that Philips is recalling its Tack Endovascular System, with the recall classified as the most serious, Class I, meaning the series of products may cause serious injury or death.

Due to serious safety concerns, this product will be completely withdrawn from the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

Image source: FDA official website

The official notice states that using the affected products could result in serious adverse health consequences, including short-term risks such as partial or complete blockage of blood flow (occlusion), holes or tears in the inner wall of the artery (dissection) that can penetrate the entire arterial wall (perforation); and long-term risks, such as pain, tissue loss, re-narrowing of the blood vessel where a stent was placed (restenosis), the need for bypass surgery, amputation, and death. Twenty injuries have been reported so far.

Specific product information is as follows:

Recalled Product

    • Product Name: 

Philips spent 2.6 billion to buy the "first and only," but it completely exited the market in less than 5 years!

01

Caused 20 people to be injured!

Another important Philips device has completely exited the market

01

Caused 20 people to be injured!

Another important Philips device has completely exited the market

01

0101

Caused 20 people to be injured!

Caused 20 people to be injured!Caused 20 people to be injured!
Another important Philips device has completely exited the market
Another important Philips device has completely exited the marketAnother important Philips device has completely exited the market

A few hours ago, the FDA officially announced that Philips is recalling its Tack endovascular system, with the recall level being the most severe, Level I, indicating that the series of products may cause serious injury or death.

A few hours ago, the FDA officially announced that Philips is recalling its Tack endovascular system, with the recall level being the most severe, Level I, indicating that the series of products may cause serious injury or death.

Due to serious safety hazards, this product will completely exit the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

Due to serious safety hazards, this product will completely exit the market. Philips urges interventional cardiologists to immediately stop using it and remove it.

image.png

image.png

Image source: FDA official website

Image source: FDA official website

The official notice states that the use of affected products may result in serious adverse health consequences, including short-term risks such as partial or complete blockage of blood flow (occlusion), holes or tears in the inner lining of an artery (dissection) and penetration through the entire arterial wall (perforation); and long-term risks, such as pain, tissue loss, expansion, or re-narrowing of a stented vessel (restenosis), the need for bypass surgery, amputation, and death. Twenty injuries have been reported so far.

The official notice states that the use of affected products may result in serious adverse health consequences, including short-term risks such as partial or complete blockage of blood flow (occlusion), holes or tears in the inner lining of an artery (dissection) and penetration through the entire arterial wall (perforation); and long-term risks, such as pain, tissue loss, expansion, or re-narrowing of a stented vessel (restenosis), the need for bypass surgery, amputation, and death. Twenty injuries have been reported so far.

The official notice states that the use of affected products may result in serious adverse health consequences, including short-term risks such as partial or complete blockage of blood flow (occlusion), holes or tears in the inner lining of an artery (dissection) and penetration through the entire arterial wall (perforation); and long-term risks, such as pain, tissue loss, expansion, or re-narrowing of a stented vessel (restenosis), the need for bypass surgery, amputation, and death. Twenty injuries have been reported so far.

Specific product information is as follows:

Specific product information is as follows:
Recalled Product

    • Product Name: 

  • Tack Endovascular System (4F,1.5-4.5mm), 150cm 

  • Tack Endovascular System (6F, 3.5 - 6.0mm), 135cm

  • Tack Endovascular System (6F, 4.0 - 8.0 mm), 135 cm

    • Unique Device Identifier (UDI)/Catalog Number: 

  • 00863328000196/154150041

  • 00863328000127/156135061 

  • 00850003494036/206135061

  • Lot Code:

  • 332905 – 349049 

  • 332824 – 336121

  • 331281 – 336152

Device Summary
Recalled Product

    • Product Name: 

  • Tack Endovascular System (4F, 1.5-4.5mm), 150cm 

  • Tack Endovascular System (6F, 3.5 - 6.0mm), 135cm

  • Tack Endovascular System (6F, 4.0 - 8.0 mm), 135 cm

    • Unique Device Identifier (UDI)/Catalog Number: 

  • 00863328000196/154150041

  • 00863328000127/156135061 

  • 00850003494036/206135061

  • Lot Code:

  • 332905 – 349049 

  • 332824 – 336121

  • 331281 – 336152

Device Summary

The Tack Endovascular System includes stents and delivery systems.

Sure, please provide the content that needs to be translated.
Recalled Product

    • Product Name:

  • Tack Endovascular System (4F, 1.5-4.5mm), 150cm

  • Tack Endovascular System (6F, 3.5 - 6.0mm), 135cm

  • Tack Endovascular System (6F, 4.0 - 8.0 mm), 135 cm

    • Unique Device Identifier (UDI)/Catalog Number:

  • 00863328000196/154150041

  • 00863328000127/156135061

  • 00850003494036/206135061

  • Lot Code:

  • 332905 – 349049

  • 332824 – 336121

  • 331281 – 336152

Device Summary

Tack Endovascular System includes stents and the delivery system, it is the world's first precise P

Recalled Product

    • Product Name:

  • Tack Endovascular System (4F,1.5-4.5mm), 150cm

  • Tack Endovascular System (6F, 3.5 - 6.0mm), 135cm

  • Tack Endovascular System (6F, 4.0 - 8.0 mm), 135 cm

    • Unique Device Identifier (UDI)/Catalog Number:

  • 00863328000196/154150041

  • 00863328000127/156135061

  • 00850003494036/206135061

  • Batch Code:

  • 332905 – 349049

  • 332824 – 336121

  • 331281 – 336152

Recalled Product
Recalled Product
Recalled Product
Recalled Product
Recalled Product

    • Product Name: 

  • Tack Endovascular System (4F,1.5-4.5mm), 150cm 

  • Tack Endovascular System (6F, 3.5 - 6.0mm), 135c

  • Tack Endovascular System (6F, 4.0 - 8.0 mm), 135 cm

    • Unique Device Identifier (UDI)/Catalog Number: 

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