Device recall
Z-0675-2008: Organogenesis Apligraf, interactive wound and burn dressing, Organogenesis…
FDA device recall · Class II · Organogenesis, Inc.
Key facts
| Recall number (Z-number) | Z-0675-2008 |
|---|---|
| Recall event | 46250 |
| Product | Organogenesis Apligraf, interactive wound and burn dressing, Organogenesis, Inc., Canton, Massachusetts 02021 |
| Product code | MGR |
| Recalling firm | Organogenesis, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 15, 2015 |
| PMA numbers | P950032 |
| FEI number | 1000148471 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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