Recall archive / FDA device enforcement
stryker Precision Thin, Catalog Number REF 2296-003-108; Micro Oscillating and Sagittal Blades — FDA record Z-1138-2025
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Jan 8, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- stryker Precision Thin, Catalog Number REF 2296-003-108; Micro Oscillating and Sagittal Blades
- Reason
- Precision Thin blade attachments have a potential to be out of measurement specifications, preventing them from securely fitting into the compatible handpiece.
- Classification
- Class II
- Recalling firm
- Stryker Corporation
- Quantity
- 622 units
- Agency-reported status
- Ongoing
- Source record identifier
- Z-1138-2025
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | GTIN 04546540046482, Lot Number 22298017 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Worldwide distribution.
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report date
- Feb 19, 2025
- Recall initiation date
- Jan 8, 2025
- Center classification date
- Feb 11, 2025
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.