Peri-Guard and Supple Peri-Guard Repair Patch
Last updated
Summary
Product
Peri-Guard and Supple Peri-Guard Repair Patch
Issue
Medical devices - Labelling and packaging
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 |
|---|---|---|
| Peri-Guard Repair Patch | All lots within expiry. | PC-1016N PC-0404N PC-0608N PC-0814N PC-1225N |
| Supple Peri-Guard Repair Patch | All lots within expiry. | PC-0608SN PC-0814SN PC-1016SN PC-0404SN |
Issue
Baxter implemented labeling changes on CE-marked Peri-Guard Repair Patch and Supple Peri-Guard Repair Patch products including removal of the indications for abdominal wall defect and hernia (diaphragmatic, femoral, incisional, inguinal, lumbar, paracolostomy, scrotal and umbilical) repair from the Instruction For Use (IFU).
Recall Start Date: April 16, 2024
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Companies
Synovis Life Technologies, Inc. A Subsidiary Of Baxter International Inc
2575 University Avenue. W., St-Paul, Minnesota, United States, 55114-1024
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-75440
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