Device recall
Z-1924-2014: Medtronic Duet External Drainage and Monitoring System, Interlink Injection…
FDA device recall · Class I · Medtronic Neurosurgery
Key facts
| Recall number (Z-number) | Z-1924-2014 |
|---|---|
| Recall event | 68503 |
| Product | Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, Lumbar Catheter, Catalog No. 46917. Intended to allow drainage and measurement of cerebrospinal fluid (CSF) and other fluids of similar physical character from the ventricles or the lumbar subarachnoid (intrathecal)… |
| Product code | JXG |
| Recalling firm | Medtronic Neurosurgery |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jan 14, 2015 |
| 510(k) numbers | K984053 |
| FEI number | 3015531529 |
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