Device recall
Z-0058-2008: Remington Medical, Inc, (RMI) -- Urinary Drainage Bags: 500ml Disposable Urinary…
FDA device recall · Class II · Remington Medical Inc.
Key facts
| Recall number (Z-number) | Z-0058-2008 |
|---|---|
| Recall event | 44938 |
| Product | Remington Medical, Inc, (RMI) -- Urinary Drainage Bags: 500ml Disposable Urinary Leg Bag (Order number: 500-D) and 1000ml Disposible Urinary Leg Bag (Order number 1000-D) -- Sterile Fluid Path, For Single Use Only, Remington Medical, Inc., Alpharetta, GA 30005. |
| Product code | EXF |
| Recalling firm | Remington Medical Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 6, 2009 |
| 510(k) numbers | K990428 |
| FEI number | 1000132370 |
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