Reported May 11, 2022 · Terminated
K-Wire, 1.35 mm x 170 mm
Arthrex, 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: Arthrex, Inc. · 1370 Creekside Blvd · Naples, FL · 34108-1945
Is this the product you have?
- K-Wire, 1.35 mm x 170 mm
- Lot codes and dates
- Part NumberAR-8610K-43
- Batch 1298116640 UDI00888867197084
- Amount recalled
- 300 pieces
Where it was sold
Why it was recalled
Products do not meet length and diameter specifications.
This product could cause temporary or reversible health problems — stop using it.
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