Ogival Interbody Cage, Peek
Ogival Interbody Cage, PEEK Recall Summary The Ogival Interbody Cage, PEEK—a spinal implant device—is being recalled in Canada due to labelling and packaging issues. This is classified as a Class I recall, which is the most serious type. The product was distributed across Canada.
- Product
- Ogival Interbody Cage, PEEK
- Reason
- Labelling and packaging
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2023-06-01
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/2e147883-7d96-434a-8105-84e4553c39f8