stryker Precision Thin, Catalog Number REF 2296-003-155; Micro Oscillating and Sagittal Blades
This recall is currently active, issued February 11, 2025. It was issued by Stryker Corporation.
- Company
- Stryker Corporation
- Recall Initiated
- January 8, 2025
- Posted
- February 11, 2025
- Recall Number
- Z-1139-2025
- Quantity
- 238 units
- Firm Location
- Portage, MI
- Official Source
- View on FDA website ↗
Reason for Recall
Precision Thin blade attachments have a potential to be out of measurement specifications, preventing them from securely fitting into the compatible handpiece.
Distribution
Worldwide distribution.
Lot / Code Info
GTIN 04546540466549, Lot Number 23070017
Root Cause
Process control
Action Taken
Stryker issued an URGENT MEDICAL DEVICE recall notice to its consignees on 01/08/2025 via FedEx. The notice explained the issue, potential risk, and requested the affected items be quarantined pending return. Stryker will issue a shipping label to the consignee once the response form has been received. Distributors were directed to forward the notice to all those to whom the affected devices were distributed.