Device recall
Z-1659-2012: Non-DEHP Microbore Administration Set with Non-Vented Spike Packaged Assembly…
FDA device recall · Class I · MOOG Medical Devices Group
Key facts
| Recall number (Z-number) | Z-1659-2012 |
|---|---|
| Recall event | 61895 |
| Product | Non-DEHP Microbore Administration Set with Non-Vented Spike Packaged Assembly, product code: 340-4114, Method of Sterilization using Ethylene Oxide. The Curlin Ambulatory Infusion Pump System with disposable PVC Administration Tubing Sets and user accessories, provide a means for the volumetric… |
| 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