FDA Device recall Z-0724-2019
Arthrex Suture Anchor, Nano Corkscrew FT (consists of an anchor pre-loaded on a handled inserter including suture, with needles.) Part Numb…
- FDA Device
- Class II
- ongoing
- Published 2019-01-23
On 2019-01-23 the FDA classified a Class II recall of Arthrex Suture Anchor, Nano Corkscrew FT (consists of an anchor pre-loaded on a handled inserter including suture, with needles.) Part Numb… by Arthrex, citing potentially lead to anchor breakage during insertion,.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0724-2019 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2018-11-19 |
| Published | 2019-01-23 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Arthrex |
| Distribution | US |
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
Potentially lead to anchor breakage during insertion,
Identifiers
| code_info | Lots #: 10175216, 1075219, 10199557, and 10199558 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0724-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.