Device recall
Z-1129-2010: 4-Way "Hi-Flo" Extension Set with Two SmartSite(TM) Y-Injection Sites and…
FDA device recall · Class I · Arrow International Inc
Key facts
| Recall number (Z-number) | Z-1129-2010 |
|---|---|
| Recall event | 54723 |
| Product | 4-Way "Hi-Flo" Extension Set with Two SmartSite(TM) Y-Injection Sites and Rotating Luer Lock SmartSite(TM) is a trademark of Alaris Medical Systems, Inc. An Intravenous Administration Tubing set is a device intended for medical purposes that consists of tubing and components with suitable adaptors… |
| Product code | FPA |
| Recalling firm | Arrow International Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Nov 8, 2012 |
| 510(k) numbers | K830755 |
| FEI number | 3015859709 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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