Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
The Covera Vascular Covered Stent is a flexible Recalled by Bard Peripheral Vascular Inc Due to An increase in the reported complaint rate for...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Bard Peripheral Vascular Inc directly.
Affected Products
The Covera Vascular Covered Stent is a flexible, self-expanding endoprothesis comprised of ePTFE encapsulating a nitinol stent framework. The inner lumen of the covered stent is carbon impregnated.
Quantity: 10,815 devices (U.S. total)
Why Was This Recalled?
An increase in the reported complaint rate for inability to deploy was identified and related to poor slide block bonding.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Bard Peripheral Vascular Inc
Bard Peripheral Vascular Inc has 136 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report