Device recall
Z-1124-2009: Medtronic Innervision Snap Shunt Ventricular Catheter, BioGlide, Catalog Number…
FDA device recall · Class I · Medtronic Neurosurgery
Key facts
| Recall number (Z-number) | Z-1124-2009 |
|---|---|
| Recall event | 51287 |
| Product | Medtronic Innervision Snap Shunt Ventricular Catheter, BioGlide, Catalog Number 27782L. Sizes: 3 CM in length, REF (240) 27782L. Each catheter is provided in a sealed Tyvek plastic tray placed within a sealed Tyvek/Mylar pouch. The sealed pouch is then placed within a chipboard carton along with… |
| Product code | JXG |
| Recalling firm | Medtronic Neurosurgery |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Nov 8, 2010 |
| 510(k) numbers | K792007, K874498, K951258 |
| FEI number | 3015531529 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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