Covera™ Vascular Covered Stent
Last updated
Summary
Product
Covera™ Vascular Covered Stent
Issue
Medical devices - Performance issue
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Affected products
| Affected products | Lot or serial number | Model or catalog number |
|---|---|---|
| Covera™ Vascular Covered Stent | ANFV0347 ANFU2250 ANFT0492 | AVFME08040 AVFME10060 AVFME07040 |
| Covera™ Vascular Covered Stent | ANFZ0861 ANFU3108 ANFY1697 ANFW0178 ANFZ0865 ANFZ0856 ANFX4113 ANFW0484 ANFW1464 ANFV1067 ANFZ0857 ANFY1703 ANFZ0854 ANFZ0855 ANFZ0860 ANFX2369 ANFW0485 ANFX4228 ANFT3594 ANFZ0864 ANFZ0866 ANFX0106 ANFV1070 | AVSME06040 AVSLE10060 AVSME06030 AVSME08060 AVSME10060 AVSLE08040 AVSLE10040 AVSLE08060 AVSME06060 AVSME08080 AVSME10080 AVSME08030 AVSME10040 AVSME08040 |
Issue
The Covera™ Vascular Covered Stent has the potential to exhibit deployment issues (i.e., failure to deploy the covered stent) due to slide block bond failures in the device handle.
Recall start date: December 28, 2022
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Companies
Angiomed Gmbh & Co. Medizintechnik Kg
Wachhausstr, 6, Karlsruhe, Baden-Wuerttemberg, Germany, 76227
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-72531
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