Device recall
Z-0764-2013: Infinity Enteralite Ambulatory Feeding Pumps, List number: INFKIT2 - Addendum to…
FDA device recall · Class II · MOOG Medical Devices Group
Key facts
| Recall number (Z-number) | Z-0764-2013 |
|---|---|
| Recall event | 63485 |
| Product | Infinity Enteralite Ambulatory Feeding Pumps, List number: INFKIT2 - Addendum to Operator's Manual Product usage: provide a means for the volumetric delivery of fluids used in Enteral applications. |
| Product code | LZH |
| Recalling firm | MOOG Medical Devices Group |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 10, 2014 |
| 510(k) numbers | K031199 |
| FEI number | 1000117172 |
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