Stryker Precision Thin (Stryker) – Blade Measurement (2025)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
stryker Precision Thin, Catalog Number REF 2296-003-108; Micro Oscillating and Sagittal Blades
Brand
Stryker Corporation
Lot Codes / Batch Numbers
GTIN 04546540046482, Lot Number 22298017
Products Sold
GTIN 04546540046482, Lot Number 22298017
Stryker Corporation is recalling stryker Precision Thin, Catalog Number REF 2296-003-108; Micro Oscillating and Sagittal Blades due to Precision Thin blade attachments have a potential to be out of measurement specifications, preventing them from securely fitting into the compatible h. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Precision Thin blade attachments have a potential to be out of measurement specifications, preventing them from securely fitting into the compatible handpiece.
Recommended Action
Per FDA guidance
Stryker issued an URGENT MEDICAL DEVICE recall notice to its consignees on 01/08/2025 via FedEx. The notice explained the issue, potential risk, and requested the affected items be quarantined pending return. Stryker will issue a shipping label to the consignee once the response form has been received. Distributors were directed to forward the notice to all those to whom the affected devices were distributed.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026