Stryker Corporation recalls stryker Precision Thin, Catalog Number REF 2296-003-108; Micro Oscillating and Sagittal Blades

Recall date

January 8, 2025

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1138-2025

FDA classification

Class II

Brand / firm

Stryker Corporation

Sold / distributed

Worldwide distribution.

Why it was recalled

Precision Thin blade attachments have a potential to be out of measurement specifications, preventing them from securely fitting into the compatible handpiece.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

stryker Precision Thin, Catalog Number REF 2296-003-108; Micro Oscillating and Sagittal Blades