Health product recall

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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