Device recall
Z-1810-2013: Medtronic Preimplantation Test Kit, Catalog No. 21047. The kit is indicated for…
FDA device recall · Class II · Medtronic Neurosurgery
Key facts
| Recall number (Z-number) | Z-1810-2013 |
|---|---|
| Recall event | 65600 |
| Product | Medtronic Preimplantation Test Kit, Catalog No. 21047. The kit is indicated for use with Medtronic CSF-Flow Control Valves and Delta Valves, when a simple preimplantation test is desired to verify that the valve conforms to labeled product specifications. |
| Product code | KYZ |
| Recalling firm | Medtronic Neurosurgery |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 23, 2013 |
| FEI number | 3015531529 |
At a glance
- None Linked 510(k)s
- 1–9 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