Device recall
Z-0476-06: Atrisorb FreeFlow Bioabsorbable Guided Tissue Regeneration (GTR) Barrier…
FDA device recall · Class II · QLT USA, Inc.
Key facts
| Recall number (Z-number) | Z-0476-06 |
|---|---|
| Recall event | 34506 |
| Product | Atrisorb FreeFlow Bioabsorbable Guided Tissue Regeneration (GTR) Barrier, Sterile |
| Product code | LYC |
| Recalling firm | QLT USA, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 27, 2006 |
| 510(k) numbers | K982865 |
| FEI number | 3001237858 |
At a glance
- 1–9 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