Drill Bit, Cannulated, 5.0 mm - Product Usage: may be used in a variety of foot and ankle procedures.
Reported: April 7, 2021 Initiated: February 24, 2021 #Z-1310-2021
Product Description
Drill Bit, Cannulated, 5.0 mm - Product Usage: may be used in a variety of foot and ankle procedures.
Reason for Recall
The color indicator on the proximal end of the shaft of the AR-8770-02 is the incorrect color.
Details
- Recalling Firm
- Arthrex, Inc.
- Units Affected
- 9 units
- Distribution
- US Nationwide distribution in the states of Ohio, Oregon, Tennessee, Texas.
- Location
- Naples, FL
Frequently Asked Questions
What product was recalled? ▼
Drill Bit, Cannulated, 5.0 mm - Product Usage: may be used in a variety of foot and ankle procedures.. Recalled by Arthrex, Inc.. Units affected: 9 units.
Why was this product recalled? ▼
The color indicator on the proximal end of the shaft of the AR-8770-02 is the incorrect color.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 7, 2021. Severity: Moderate. Recall number: Z-1310-2021.
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