Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile… — Class II medical device recall Z-0919-2020
Terminated recall by Arthrex, Inc., reported 2020-02-05, distributed nationwide. There is a potential for blockage of the Hub Attachment Tube.
| Recall number | Z-0919-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arthrex, Inc., Naples, FL, United States |
| Recall initiated | 2019-12-17 |
| Classified | 2020-01-30 |
| Reported by FDA | 2020-02-05 |
| Terminated | 2023-08-31 |
| Distributed | Nationwide (US) |
| Quantity | 47 |
| Lot numbers | 051838 |
Product
Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile instruments Outrigger Targeting Guide
Reason for recall
There is a potential for blockage of the Hub Attachment Tube.
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-0919-2020. 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.