Drill Bit — Class II medical device recall Z-1310-2021
Terminated recall by Arthrex, Inc., reported 2021-04-07, distributed nationwide. The color indicator on the proximal end of the shaft of the AR-8770-02 is the incorrect color.
| Recall number | Z-1310-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arthrex, Inc., Naples, FL, United States |
| Recall initiated | 2021-02-24 |
| Classified | 2021-03-26 |
| Reported by FDA | 2021-04-07 |
| Terminated | 2023-05-02 |
| Distributed | Nationwide (US) |
| Quantity | 9 units |
| Lot numbers | 032052 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1310-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.