Device recall
Z-0390-05: Zimmer™ Orthopaedic Surgical Products, Disposable Cuff, 12'' (30cm), Dual Port…
FDA device recall · Class II · Zimmer Orthopaedic Surgical Products
Key facts
| Recall number (Z-number) | Z-0390-05 |
|---|---|
| Recall event | 30476 |
| Product | Zimmer™ Orthopaedic Surgical Products, Disposable Cuff, 12'' (30cm), Dual Port, Single Bladder Sterile, Zimmer, Dover, OH USA. The cuff is a sterile, single use product equipped with an integral fill line. The product is packed 10 cuffs per unit. |
| Product code | KCY |
| Recalling firm | Zimmer Orthopaedic Surgical Products |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 20, 2005 |
| FEI number | 1035617 |
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