Device recall
Z-2339-2016: Zimmer Air Dermatome II Width Plate, 3 inch. Part #00-8851-203-00. Width plate…
FDA device recall · Class II · Zimmer Surgical Inc
Key facts
| Recall number (Z-number) | Z-2339-2016 |
|---|---|
| Recall event | 74636 |
| Product | Zimmer Air Dermatome II Width Plate, 3 inch. Part #00-8851-203-00. Width plate is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag, which is then placed into a… |
| Product code | GFD |
| Recalling firm | Zimmer Surgical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 21, 2017 |
| 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