Device recall
Z-2306-2008: Corflo Anti-I.V. NG Tube for Pediatric and Neonatal Use; a sterile clear…
FDA device recall · Class III · Cardinal Health
Key facts
| Recall number (Z-number) | Z-2306-2008 |
|---|---|
| Recall event | 48726 |
| Product | Corflo Anti-I.V. NG Tube for Pediatric and Neonatal Use; a sterile clear polyurethane with orange radiopaque stripe Enteral Feeding Tube without Stylet, 5 Fr, 22" long, non-weighted, DEHP and latex free; individually packaged, 10 tubes per carton; Mfg. by Viasys MedSystems, Wheeling, IL 60090… |
| Product code | KNT |
| Recalling firm | Cardinal Health |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 26, 2008 |
| 510(k) numbers | K043044 |
| FEI number | 3001236905 |
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