Device recall
Z-1794-2009: Alaris System Inter-Unit Interface (IUI) Connectors. The Modules include the…
FDA device recall · Class I · Cardinal Health 303 dba Cardinal Health
Key facts
| Recall number (Z-number) | Z-1794-2009 |
|---|---|
| Recall event | 52119 |
| Product | Alaris System Inter-Unit Interface (IUI) Connectors. The Modules include the following: Alaris PC Unit, Model Numbers 8000 and 8015; Alaris Pump Module, Model 8100; Alaris Patient-Controlled Analgesia (PCA), Model 8120; Alaris Syringe Module, Model 8110; Alaris SpO2 Module, Model 8210 and 8220 and… |
| Product code | FRN |
| Recalling firm | Cardinal Health 303 dba Cardinal Health |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Mar 19, 2012 |
| 510(k) numbers | K012383, K023264, K032233 |
| FEI number | 2016493 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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