Drill Bit, Cannulated, 5.0 mm - Product Usage: may be used in a variety of foot and ankle procedures.
This recall has been terminated (originally issued February 24, 2021).
- Company
- Arthrex, Inc.
- Recall Initiated
- February 24, 2021
- Terminated
- May 2, 2023
- Recall Number
- Z-1310-2021
- Quantity
- 9 units
- Firm Location
- Naples, FL
- Official Source
- View on FDA website ↗
Reason for Recall
The color indicator on the proximal end of the shaft of the AR-8770-02 is the incorrect color.
Distribution
US Nationwide distribution in the states of Ohio, Oregon, Tennessee, Texas.
Lot / Code Info
Product Code AR-8770-02, Lot Number 032052
Root Cause
Under Investigation by firm
Action Taken
Consignees were notified via e-mail with URGENT: RECALL NOTIFICATION dated 02/23/2021. The letter identified affected product, reason for recall, and instructed consignee to immediately discontinue use, sale, and distribution of the product as well instructions for handling of affected product.
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