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Arthrex, Inc. recalls Drill Bit, Cannulated, 5.0 mm - Product Usage: may be used in a variety of foot and ankle procedures.
Recalled April 7, 2021 · FDA recall Z-1310-2021 · Arthrex
Hazard
The color indicator on the proximal end of the shaft of the AR-8770-02 is the incorrect color. · FDA Class II
Units
9 units
Sold at
US Nationwide distribution in the states of Ohio, Oregon, Tennessee, Texas.
Description
The color indicator on the proximal end of the shaft of the AR-8770-02 is the incorrect color.
Product
Drill Bit, Cannulated, 5.0 mm - Product Usage: may be used in a variety of foot and ankle procedures.
Manufacturer(s)
Arthrex, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →