Device recall
Z-0460-2008: Cardinal Health Alaris Pump Module (formerly Medley Pump Module), Model 8100…
FDA device recall · Class I · Cardinal Health 303 Inc DBA Alaris Products
Key facts
| Recall number (Z-number) | Z-0460-2008 |
|---|---|
| Recall event | 45504 |
| Product | Cardinal Health Alaris Pump Module (formerly Medley Pump Module), Model 8100, Cardinal Health, San Diego, CA. (All Alaris Pump modules shipped prior to December 23, 2007 are subject to this recall) |
| Product code | FRN |
| Recalling firm | Cardinal Health 303 Inc DBA Alaris Products |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jun 6, 2011 |
| FEI number | 3003879246 |
At a glance
- None 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