Device recall
Z-1768-2022: ORCA FOAM STANDARD CUBE 10x10x10 mm, Absorbable Gelatin Sponge Hemostat, USP…
FDA device recall · Class II · GELITA MEDICAL GMBH
Key facts
| Recall number (Z-number) | Z-1768-2022 |
|---|---|
| Recall event | 90743 |
| Product | ORCA FOAM STANDARD CUBE 10x10x10 mm, Absorbable Gelatin Sponge Hemostat, USP, REF ORCA FOAM |
| Product code | LYA |
| Recalling firm | GELITA MEDICAL GMBH |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 22, 2026 |
| 510(k) numbers | K060878 |
| FEI number | 3010208179 |
At a glance
- 1–9 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