FDA recall Z-1138-2025

Stryker Corporation · Class II · device

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.

Distribution

Worldwide distribution.

Key facts

Status: Ongoing
Initiation date: 2025-01-08
Report date: 2025-02-19
Voluntary/Mandated: Voluntary: Firm initiated
Location: Portage, MI, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1138-2025