Modular Cathcart Fracture Head
Recall Summary The Modular Cathcart Fracture Head, a medical device used in orthopedic surgery, is being recalled in Canada due to labelling and packaging issues. This is a Class I recall, indicating a serious safety concern. The product was distributed across Canada.
- Product
- Modular Cathcart Fracture Head
- Reason
- Labelling and packaging
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2022-06-20
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/64eaa6d3-9b51-4484-9bd2-83096cbb62fa