Device recall
Z-2674-2014: DePuy Synthes TI Vectra Plates: TI Vectra-One" Plate 2 Level / 34 mm part…
FDA device recall · Class II · Synthes, Inc.
Key facts
| Recall number (Z-number) | Z-2674-2014 |
|---|---|
| Recall event | 69178 |
| Product | DePuy Synthes TI Vectra Plates: TI Vectra-One" Plate 2 Level / 34 mm part 04.613.184 3337672 TI Vectra" Plate 3 Level / 57 mm part 04.613.257 lot 3693878 TI Vectra" Plate 4 Level / 64 mm part 04.613.364 lot 8143905 |
| Product code | KWQ |
| Recalling firm | Synthes, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 2, 2015 |
| 510(k) numbers | K050451, K071667 |
| FEI number | 3005180112 |
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