Device recall
Z-0526-2019: NEOCONNECT, Enteral Extension with ENFit connector, REF EXT-60NC The NeoMed…
FDA device recall · Class III · Neomed Inc
Key facts
| Recall number (Z-number) | Z-0526-2019 |
|---|---|
| Recall event | 81452 |
| Product | NEOCONNECT, Enteral Extension with ENFit connector, REF EXT-60NC The NeoMed NeoConnect Enteral Only Extension Set is intended for use as an extension set for nasogastric/oralgastric or gastric tube enteral feeding tubes, incorporating safety connectors which help mitigate the risk of accidental… |
| Product code | KNT |
| Recalling firm | Neomed Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 16, 2020 |
| 510(k) numbers | K100288 |
| 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