Device recall
Z-0724-2019: Arthrex Suture Anchor, Nano Corkscrew FT (consists of an anchor pre-loaded on a…
FDA device recall · Class II · Arthrex, Inc.
Key facts
| Recall number (Z-number) | Z-0724-2019 |
|---|---|
| Recall event | 81819 |
| 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 |
| Product code | MBI |
| Recalling firm | Arthrex, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K180118 |
| FEI number | 1220246 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database