Device recall
Z-0688-2016: Moog Curlin Infusion, Ambulatory Infusion Pump The Curlin Ambulatory Infusion…
FDA device recall · Class II · MOOG Medical Devices Group
Key facts
| Recall number (Z-number) | Z-0688-2016 |
|---|---|
| Recall event | 72923 |
| Product | Moog Curlin Infusion, Ambulatory Infusion Pump The Curlin Ambulatory Infusion System includes Curlin Ambulatory multi-therapy and PainSmart pumps. Curlin 4000, catalog number 340; Curlin 6000, 6000 CMS, and PainSmart IOD, catalog number 360; and Curlin Pump Calibration Set, catalog number 340-4038. |
| Product code | FRN |
| Recalling firm | MOOG Medical Devices Group |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 21, 2017 |
| 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