Reported Dec 29, 2021 · Ongoing
Stryker CLAW II ORTHOLOC 3DSi Plate, Hole Qty: 4, 30mm, REF 40240430.
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 · 11576 Memphis Arlington Rd · Arlington, TN · 38002-9497
Is this the product you have?
- Stryker CLAW II ORTHOLOC 3DSi Plate
- Hole Qty
430mmREF 40240430
- Lot codes and dates
- Lot #1642103
- Amount recalled
- 23 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
Why it was recalled
The incorrect product is contained in the packaging.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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