stryker Precision Thin — Class II medical device recall Z-1138-2025
Ongoing recall by Stryker Corporation, reported 2025-02-19. Precision Thin blade attachments have a potential to be out of measurement specifications, preventing them fro
| Recall number | Z-1138-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Corporation, Portage, MI, United States |
| Recall initiated | 2025-01-08 |
| Classified | 2025-02-11 |
| Reported by FDA | 2025-02-19 |
| Quantity | 622 units |
| UPC / GTIN / UDI-DI | 04546540046482 |
| Lot numbers | 22298017 |
| Model numbers | 2296-003-108 |
Product
stryker Precision Thin, Catalog Number REF 2296-003-108; Micro Oscillating and Sagittal Blades
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1138-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.