Device recall
Z-1277-2018: CORTRAK* 2 Nasogastric/Nasointestinal (NG/NI) Feeding Tubes with Electromagnetic…
FDA device recall · Class II · Halyard Health, Inc
Key facts
| Recall number (Z-number) | Z-1277-2018 |
|---|---|
| Recall event | 79479 |
| Product | CORTRAK* 2 Nasogastric/Nasointestinal (NG/NI) Feeding Tubes with Electromagnetic Transmitting Stylet and CORFLO* Enteral Feeding tube, ANTI-IV* Connector, 10 Fr, 140 cm The device is used in patients that require intermittent or continuous tube feedings via the nasogastric or nasoenteric route. |
| Product code | FPB |
| Recalling firm | Halyard Health, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 4, 2021 |
| 510(k) numbers | K083210 |
| FEI number | 3011270181 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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