Device recall
Z-1080-2012: CORFLO-Ultra Jejunal Tube with CORLOCK-Twoomey Y-Adaptor for use with the…
FDA device recall · Class II · Corpak Med Systems
Key facts
| Recall number (Z-number) | Z-1080-2012 |
|---|---|
| Recall event | 61036 |
| Product | CORFLO-Ultra Jejunal Tube with CORLOCK-Twoomey Y-Adaptor for use with the CORFLO-Max PEG; enteral feeding tube,10 Fr, 36" (91 cm), 3 Gram weighted bolus; individually packaged, 5 tubes per case; CORPAK MedSystems, Wheeling, IL 60090; catalog/reorder #30-7361; For delivery of enteral nutrition… |
| Product code | KNT |
| Recalling firm | Corpak Med Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 21, 2012 |
| 510(k) numbers | K821906 |
| FEI number | 3011270181 |
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