Device recall
Z-2188-2010: CLAW HEX SCREW CHARLOTTE " F&A SYSTEM CONTENTS: 1 EACH Foot and Ankle Screw…
FDA device recall · Class II · Wright Medical Technology Inc
Key facts
| Recall number (Z-number) | Z-2188-2010 |
|---|---|
| Recall event | 56091 |
| Product | CLAW HEX SCREW CHARLOTTE " F&A SYSTEM CONTENTS: 1 EACH Foot and Ankle Screw ... IMPLANT MATERIAL: Stainless Steel Ref: 4013-3520 ... Size 3.5MM, Length 20 MM, Use with Clava 3.5MM - Non-Sterile. Implantation: used in Food and Ankle surgeries. |
| Product code | HRS |
| Recalling firm | Wright Medical Technology Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 23, 2011 |
| 510(k) numbers | K080295 |
| FEI number | 1043534 |
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