Device recall
Z-0415-2016: Catalog No. INF0020-A EnteraLite Infinity Enteral Pump Delivery Set with ENFit…
FDA device recall · Class II · MOOG Medical Devices Group
Key facts
| Recall number (Z-number) | Z-0415-2016 |
|---|---|
| Recall event | 72682 |
| Product | Catalog No. INF0020-A EnteraLite Infinity Enteral Pump Delivery Set with ENFit Connector System and Transitional Stepped Connector (spiked set); Catalog No. INF0500-A - 500ml EnteraLite Infinity Enteral Pump Delivery Set with ENFit Connector System and Transitional Stepped Connector; Catalog No… |
| Product code | PIF |
| Recalling firm | MOOG Medical Devices Group |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 22, 2016 |
| 510(k) numbers | K142539 |
| FEI number | 1000117172 |
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