Device recall
Z-0055-06: Dual Lumen Cannula, 12Fr., sterile, disposable. Manufactured by OriGen…
FDA device recall · Class III · Origen Biomedical, Inc
Key facts
| Recall number (Z-number) | Z-0055-06 |
|---|---|
| Recall event | 31526 |
| Product | Dual Lumen Cannula, 12Fr., sterile, disposable. Manufactured by OriGen Biomedical, 4020 S. Industrial Dr. #160, Austin, Texas USA 78744 |
| Product code | DQO |
| Recalling firm | Origen Biomedical, Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 3, 2005 |
| FEI number | 1000160256 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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