Device recall
Z-1133-2022: INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 NAIL 13mm X 42cm 130DEG…
FDA device recall · Class II · Smith & Nephew Orthopaedics GmbH
Key facts
| Recall number (Z-number) | Z-1133-2022 |
|---|---|
| Recall event | 90118 |
| Product | INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Right |
| Product code | JDS |
| Recalling firm | Smith & Nephew Orthopaedics GmbH |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K040212 |
| FEI number | 3002465897 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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