Device recall
Z-1899-2008: Model 6000 CMS, CMS IOD, or Plus Ambulatory Infusion Pump, Model Number…
FDA device recall · Class II · Curlin Medical Llc
Key facts
| Recall number (Z-number) | Z-1899-2008 |
|---|---|
| Recall event | 48639 |
| Product | Model 6000 CMS, CMS IOD, or Plus Ambulatory Infusion Pump, Model Number: 360-1101 |
| Product code | FRN |
| Recalling firm | Curlin Medical Llc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 11, 2009 |
| 510(k) numbers | K981816 |
| FEI number | 3002936294 |
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