Arthrex Suture Anchor — Class II medical device recall Z-0724-2019
Ongoing recall by Arthrex, Inc., reported 2019-01-23, distributed nationwide. Potentially lead to anchor breakage during insertion,
| Recall number | Z-0724-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arthrex, Inc., Naples, FL, United States |
| Recall initiated | 2018-11-19 |
| Classified | 2019-01-11 |
| Reported by FDA | 2019-01-23 |
| Distributed | Nationwide (US) |
| Countries outside the US | DE, FI |
| Reason classes | device malfunction |
| Lot numbers | 10175216, 10199557, 10199558, 1075219 |
| Model numbers | AR-1317FT |
Product
Arthrex Suture Anchor, Nano Corkscrew FT (consists of an anchor pre-loaded on a handled inserter including suture, with needles.) Part Number AR-1317FT Product Usage: Soft tissue fixation to bone in the hand and wrist
Reason for recall
Potentially lead to anchor breakage during insertion,
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-0724-2019. 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.