Device recall
Z-1403-2012: Epidural Administration Set with Non-Vented Bag Spike and 0.2 Micron Filter…
FDA device recall · Class II · MOOG Medical Devices Group
Key facts
| Recall number (Z-number) | Z-1403-2012 |
|---|---|
| Recall event | 61446 |
| Product | Epidural Administration Set with Non-Vented Bag Spike and 0.2 Micron Filter Packaged Assembly The Curlin Ambulatory Infusion Pump System with disposable PVC Administration Tubing Sets and user accessories, provide a means for the volumetric delivery of fluids used in Parenteral, Enteral, Epidural… |
| Product code | FRN |
| Recalling firm | MOOG Medical Devices Group |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 26, 2012 |
| FEI number | 1000117172 |
At a glance
- None Linked 510(k)s
- 10–99 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