Device recall
Z-2328-2008: Integra Dermal Regeneration Template; 8 x 10 in (20 cm x 25 cm), Sterile…
FDA device recall · Class III · Integra LifeSciences Corp
Key facts
| Recall number (Z-number) | Z-2328-2008 |
|---|---|
| Recall event | 48964 |
| Product | Integra Dermal Regeneration Template; 8 x 10 in (20 cm x 25 cm) , Sterile; Integra LifeSciences Corporation, 311 Enterprise Drive, Plainsboro, NJ 08536 USA |
| Product code | MDD |
| Recalling firm | Integra LifeSciences Corp |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 22, 2008 |
| PMA numbers | P900033 |
| FEI number | 1121308 |
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