Device recall
Z-1668-2012: Non-DEHP Epidural Admin Set with 0.2 Micron Filter Non-Vented Bag Spike ASV…
FDA device recall · Class I · MOOG Medical Devices Group
Key facts
| Recall number (Z-number) | Z-1668-2012 |
|---|---|
| Recall event | 61895 |
| Product | Non-DEHP Epidural Admin Set with 0.2 Micron Filter Non-Vented Bag Spike ASV Packaged, product code: 340-4165, Method of Sterilization using Ethylene Oxide. |
| Product code | FPK |
| Recalling firm | MOOG Medical Devices Group |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Feb 22, 2013 |
| 510(k) numbers | K981816 |
| FEI number | 1000117172 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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