Catalyft™ Pl Expandable Interbody System, Interbody Cage
Recall Summary Catalyft™ PL Expandable Interbody System devices are being recalled across Canada due to performance issues. This recall affects an interbody cage product used in spinal surgery. The FDA has classified this as a Class I recall, indicating a serious concern related to how the device functions.
- Product
- Catalyft™ PL Expandable Interbody System, Interbody Cage
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2025-10-14
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/ed13c384-14da-4221-982c-07b4f573680c