Stryker Corporation: Medical Device Recall in 2025 - (Recall #: Z-1139-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: January 8, 2025

Date Posted: February 19, 2025

Recall Number: Z-1139-2025

Event ID: 96098

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.

Status: Ongoing

Product Quantity: 238 units

Code Information:

GTIN 04546540466549, Lot Number 23070017

Distribution Pattern:

Worldwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated