Device recall
Z-1625-2012: 50 Portal Vein Cannula REF 61.110.10.030 Size: Fr 10 Length: 12 Inches LL…
FDA device recall · Class II · MEDDEV USA, INC.
Key facts
| Recall number (Z-number) | Z-1625-2012 |
|---|---|
| Recall event | 61859 |
| Product | 50 Portal Vein Cannula REF 61.110.10.030 Size: Fr 10 Length: 12 Inches LL Connector LOT 120493 NON STERILE MEDDEV USA, INC. 100 Highland Park Village/Suite 200 DALLAS, TEXAS 75205 For use in humans. No indication of use is on the label. However, the device can be used for infusion. |
| Product code | KDH |
| Recalling firm | MEDDEV USA, INC. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 15, 2013 |
| FEI number | 3009257101 |
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