Device recall
Z-0218-2008: Texium Closed Male Luer (CML), Model Number 10012241, Cardinal Health, SanDiego…
FDA device recall · Class II · Cardinal Health 303 Inc DBA Alaris Products
Key facts
| Recall number (Z-number) | Z-0218-2008 |
|---|---|
| Recall event | 44826 |
| Product | Texium Closed Male Luer (CML), Model Number 10012241, Cardinal Health, SanDiego, CA. |
| Product code | FPA |
| Recalling firm | Cardinal Health 303 Inc DBA Alaris Products |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 28, 2012 |
| 510(k) numbers | K053049 |
| FEI number | 3003879246 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ 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