Device recall
Z-1115-2010: 15 Drop IV Sets, with Retractable Luer-Lock and with Smartsite(TM) Y-Injection…
FDA device recall · Class I · Arrow International Inc
Key facts
| Recall number (Z-number) | Z-1115-2010 |
|---|---|
| Recall event | 54723 |
| Product | 15 Drop IV Sets, with Retractable Luer-Lock and with Smartsite(TM) Y-Injection sites and 4-Way Stopcock with Pressure Activated Valve Manifold. (Approx. 15 drops/ml). An Intravenous Administration Tubing set is a device intended for medical purposes that consists of tubing and components with… |
| 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