Device recall
Z-1040-04: Synchromed II infusion pump
FDA device recall · Class II · Medtronic Inc, Neurological & Spinal Division
Key facts
| Recall number (Z-number) | Z-1040-04 |
|---|---|
| Recall event | 29297 |
| Product | Synchromed II infusion pump |
| Product code | FRN |
| Recalling firm | Medtronic Inc, Neurological & Spinal Division |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 23, 2005 |
| PMA numbers | P860004, P860004/060 |
| FEI number | 2182207 |
At a glance
- None 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