Device recall
Z-0648-05: Latex Free*** REF B1000P Belly Bag Urine Collection Bag with Sample Port***1000…
FDA device recall · Class III · Teleflex Medical, Inc.
Key facts
| Recall number (Z-number) | Z-0648-05 |
|---|---|
| Recall event | 31009 |
| Product | Latex Free*** REF B1000P Belly Bag Urine Collection Bag with Sample Port***1000 ml LOT***Sterile EO*** Single use only, Manufactured and Distributed by***Rusch Inc., 245 Meadowbrook Parkway, Duluth, GA 30096***Quantity 10**** |
| Product code | KNX |
| Recalling firm | Teleflex Medical, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 31, 2009 |
| FEI number | 2429473 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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