Device recall
Z-0362-2008: VKS Tibial Trial, Right/Left, Prep Guide; Model Number: 1214331, 1214332…
FDA device recall · Class II · Plus Orthopedics USA
Key facts
| Recall number (Z-number) | Z-0362-2008 |
|---|---|
| Recall event | 45484 |
| Product | VKS Tibial Trial, Right/Left, Prep Guide; Model Number: 1214331, 1214332, 1214333, 1214334, 1214335: ( Model Number: 1214331 VKS Tibial Prep Guide, Right/Left, Size 1, Lot Code EM. 1 and EM.6; 1214332 VKS Tibial Prep Guide, Right/Left, Size 2 Lot Code EM.l and EM.6, 1214333 VKS Tibial Prep Guide… |
| Product code | JWH |
| Recalling firm | Plus Orthopedics USA |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 13, 2007 |
| FEI number | 3001237832 |
At a glance
- None 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