Z-1139-2025 Class II Ongoing
FDA device recall Z-1139-2025 was initiated by Stryker Corporation on January 8, 2025 and is designated Class II. 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. The recall status is ongoing. Affected quantity: 238 units.
Recall Details
- Product Type
- Devices
- Report Date
- February 19, 2025
- Initiation Date
- January 8, 2025
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 238 units
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.
Distribution Pattern
Worldwide distribution.
Code Information
GTIN 04546540466549, Lot Number 23070017