Device recall
Z-1711-2008: Grey Inter-Unit Interface Connectors ("IUI") on the following Alaris System…
FDA device recall · Class II · Cardinal Health 303 Inc DBA Alaris Products
Key facts
| Recall number (Z-number) | Z-1711-2008 |
|---|---|
| Recall event | 47335 |
| Product | Grey Inter-Unit Interface Connectors ("IUI") on the following Alaris System modules built on or before March 26, 2004: (1) Alaris PC point-of-care unit ("PC Unit") (Model 8000)* (a.k.a. Medley PC Unit), (2) Alaris Pump Module (Model 8100) (a.k.a. Medley Pump Module), (3) Alaris Syringe Module (Model… |
| Product code | FRN |
| Recalling firm | Cardinal Health 303 Inc DBA Alaris Products |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 13, 2011 |
| 510(k) numbers | K010966, K012383, K022677, K023264, K043299 |
| FEI number | 3003879246 |
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