Device recall
Z-0581-04: One Way Valve/Female to Male Flow, 22 mm I.D./22 mm O.D., Ref 396798, Lot ***…
FDA device recall · Class II · Rusch Inc
Key facts
| Recall number (Z-number) | Z-0581-04 |
|---|---|
| Recall event | 28260 |
| Product | One Way Valve/Female to Male Flow, 22 mm I.D./22 mm O.D., Ref 396798, Lot ***, SINGLE USE ONLY, Latex Free, Quantity 50 Each Manufactured for and Distributed by RUSCH 2450 Meadowbrook Parkway, Duluth, GA 30098, Made in Taiwan. |
| Product code | CBP |
| Recalling firm | Rusch Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 21, 2006 |
| FEI number | 2429473 |
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