Device recall
Z-0093-2019: NeoMed Enteral Feeding Tubes with Enteral Only Connectors, French sizes 4.0Fr…
FDA device recall · Class II · Neomed Inc
Key facts
| Recall number (Z-number) | Z-0093-2019 |
|---|---|
| Recall event | 81116 |
| Product | NeoMed Enteral Feeding Tubes with Enteral Only Connectors, French sizes 4.0Fr, 5.0Fr, 6.5Fr, 8.0Fr, and lengths 40cm, 60cm, 90cm. The product consists of a polyurethane feeding tube with an attached hub and tethered plug to close the hub when the feeding tube is not in use. Product Usage: Intended… |
| Product code | FPD |
| Recalling firm | Neomed Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 21, 2020 |
| 510(k) numbers | K082238 |
| FEI number | 3011270181 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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