Device recall
Z-2163-2017: CORFLO PEG Kit, Pull 16FR. Product Usage: CORFLO PEG Tubes are intended for…
FDA device recall · Class II · CORPAK MedSystems, Inc.
Key facts
| Recall number (Z-number) | Z-2163-2017 |
|---|---|
| Recall event | 76465 |
| Product | CORFLO PEG Kit, Pull 16FR. Product Usage: CORFLO PEG Tubes are intended for delivery of enteral nutrition, water and medications into the stomach. The PEG adapter is the connection point between the tubing and the feeding set/syringe. The adapter is designed as a replaceable component. |
| Product code | KNT |
| Recalling firm | CORPAK MedSystems, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 5, 2019 |
| 510(k) numbers | K882867 |
| 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