PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: February 19, 2025 Initiated: January 8, 2025 #Z-1139-2025

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.

Details

Recalling Firm
Stryker Corporation
Units Affected
238 units
Distribution
Worldwide distribution.
Location
Portage, MI

Frequently Asked Questions

What product was recalled?
stryker Precision Thin, Catalog Number REF 2296-003-155; Micro Oscillating and Sagittal Blades. Recalled by Stryker Corporation. Units affected: 238 units.
Why was this product recalled?
Precision Thin blade attachments have a potential to be out of measurement specifications, preventing them from securely fitting into the compatible handpiece.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 19, 2025. Severity: Moderate. Recall number: Z-1139-2025.