Device recall
Z-1035-2009: Integra Dermal Regeneration Template-TS Catalog number 32021 Catalog number…
FDA device recall · Class II · Integra LifeSciences Corp
Key facts
| Recall number (Z-number) | Z-1035-2009 |
|---|---|
| Recall event | 50899 |
| Product | Integra Dermal Regeneration Template-TS Catalog number 32021 Catalog number 82021 |
| Product code | MDD |
| Recalling firm | Integra LifeSciences Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 25, 2009 |
| 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