FDAClass IIFebruary 19, 2025

stryker Precision Thin recall

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

Why was stryker Precision Thin recalled?

Precision Thin blade attachments have a potential to be out of measurement specifications, preventing them from securely fitting into the compatible handpiece.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

GTIN 04546540466549, Lot Number 23070017

Product
stryker Precision Thin, Catalog Number REF 2296-003-155; Micro Oscillating and Sagittal Blades
Recalling firm
Stryker Corporation
Quantity
238 units
Distribution
Worldwide distribution.
Recall date
February 19, 2025
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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