Device recall
Z-1140-2009: Snap Shunt Ventricular Catheter, Standard, with BioGlide, 3 CM, Ref 27708F. Each…
FDA device recall · Class I · Medtronic Neurosurgery
Key facts
| Recall number (Z-number) | Z-1140-2009 |
|---|---|
| Recall event | 51287 |
| Product | Snap Shunt Ventricular Catheter, Standard, with BioGlide, 3 CM, Ref 27708F. 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 IFU and patient wallet cards. The product is ETO… |
| 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