Device recall
Z-1483-2013: The Zimmer Air Dermatome, REF 00- 8801- 001- 00, Rx, non-sterile grafting…
FDA device recall · Class II · Zimmer Surgical Inc
Key facts
| Recall number (Z-number) | Z-1483-2013 |
|---|---|
| Recall event | 65258 |
| Product | The Zimmer Air Dermatome, REF 00- 8801- 001- 00 , Rx, non-sterile grafting instruments intended to provide variable graft thickness and width capabilities |
| Product code | GFD |
| Recalling firm | Zimmer Surgical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 15, 2014 |
| FEI number | 1526350 |
At a glance
- None 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