Class II

Medical Device Recall: stryker Precision Thin, Catalog Number REF 2296-003-155; Micro Oscillating and Sagittal Blades

Stryker Corporation · January 8, 2025

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.

Quantity Affected

238 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1139-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Stryker Corporation Medical Device Recall: stryker Precision Thin, Catalog Number REF 2296-003-155; Micro Oscillating and Sagittal Blades | SafeCheck