Health product recall

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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