Reported Mar 8, 2023 · Ongoing
ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 40241425, Bone fixation device
Wright Medical Technology, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Wright Medical Technology, Inc. · 1023 Cherry Rd · Memphis, TN · 38117-5423
Is this the product you have?
ORTHOLOC 3DSi CLAW II 4 HOLE PlateSize 25MMREF 40241425Bone fixation device
- Lot codes and dates
GTIN 00840420110770Lot Number 1636042
- Amount recalled
- 4 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
- NY
Why it was recalled
Stryker has identified an issue that impacts two specific lots of CLAW" II plates. The plates within these two lots were found to have been comingled, resulting in the incorrect product in packages. Packaging for 402S0425 incorrectly contained 40241425, and vice versa.
This product could cause temporary or reversible health problems — stop using it.
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