Reported Apr 7, 2021 · Terminated
Drill Bit, Cannulated, 5.0 mm - Product Usage: may be used in a variety of foot and ankle procedures.
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?
- Drill Bit, Cannulated, 5.0
- mm - Product Usagemay be used in a variety of foot and ankle procedures
- Lot codes and dates
Product Code AR-8770-02Lot Number 032052
- Amount recalled
- 9 units
Where it was sold
Why it was recalled
The color indicator on the proximal end of the shaft of the AR-8770-02 is the incorrect color.
This product could cause temporary or reversible health problems — stop using it.
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