V-loc™ 90 And 180 Suture Products
V-Loc™ 90 and 180 Suture Products Recall V-Loc™ 90 and 180 suture products are being recalled across Canada due to a sterility concern. These surgical sutures may not be sterile as intended. The recall is classified as Class II, meaning the product could cause adverse health effects but is unlikely to cause serious injury.
- Product
- V-Loc™ 90 and 180 Suture Products
- Reason
- Sterility concern
- Classification
- Class II
- Category
- medical device recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2026-07-16
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/a18e4a86-9e5f-4915-ac54-4413e514c586