Device recall
Z-2053-2019: MOOG Curlin Infusion Administration Set, REF 340-4130, Non-DEHP Tubing with…
FDA device recall · Class II · Zevex Incorporated (dba MOOG Medical Devices Group)
Key facts
| Recall number (Z-number) | Z-2053-2019 |
|---|---|
| Recall event | 82864 |
| Product | MOOG Curlin Infusion Administration Set, REF 340-4130, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron Filter, packaged 20 sets/carton, sterile. Product Usage: Administration set to be used with the Moog Curlin Infusion Pump. The pump can be used for intravenous, intra-arterial… |
| Product code | FRN |
| Recalling firm | Zevex Incorporated (dba MOOG Medical Devices Group) |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 28, 2021 |
| 510(k) numbers | K981816 |
| 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