Recall Z-1139-2025— Stryker Corporation

Name: FDA recall Z-1139-2025
Creator: U.S. Food and Drug Administration
Published: 2025-01-08

Class II · Ongoing

Class II FDA medical device recall by Stryker Corporation, initiated 2025-01-08. FDA's recall record names no specific 510(k) clearance for this event. Product: stryker Precision Thin, Catalog Number REF 2296-003-155; 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..

Recalling firm: Stryker Corporation
Classification: Class II
Status: Ongoing
Initiated: 2025-01-08
Firm location: Portage, MI, United States

Product description

stryker Precision Thin, Catalog Number REF 2296-003-155; 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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.