Device recall
Z-2405-2011: Drainage Bag, Model 600D, 600 mL, Single use, Ethylene Oxide sterilized…
FDA device recall · Class III · Remington Medical Inc.
Key facts
| Recall number (Z-number) | Z-2405-2011 |
|---|---|
| Recall event | 58664 |
| Product | Drainage Bag, Model 600D, 600 mL, Single use, Ethylene Oxide sterilized, Remington Medical, Inc., 6830 Meadowridge Court, Alpharetta, GA 30005. The Biliary Drainage Bag is used to aid with fluid drainage involving abscess, biliary and nephrostomy. Mechanical failure of this device would result in… |
| Product code | EXF |
| Recalling firm | Remington Medical Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 13, 2011 |
| FEI number | 1000132370 |
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