Drill Bit recall
Drill Bit, Cannulated, 5.0 mm - Product Usage: may be used in a variety of foot and ankle procedures.
Why was Drill Bit recalled?
The color indicator on the proximal end of the shaft of the AR-8770-02 is the incorrect color.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Product Code AR-8770-02, Lot Number 032052
- Product
- Drill Bit, Cannulated, 5.0 mm - Product Usage: may be used in a variety of foot and ankle procedures.
- Recalling firm
- Arthrex, Inc.
- Quantity
- 9 units
- Distribution
- US Nationwide distribution in the states of Ohio, Oregon, Tennessee, Texas.
- Recall date
- April 7, 2021
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)