Device recall
Z-1159-06: Medtronic Zinetics Manometric Catheter, Model 9012P2271. Water perfused…
FDA device recall · Class III · Medtronic Gastroenterology / Urology
Key facts
| Recall number (Z-number) | Z-1159-06 |
|---|---|
| Recall event | 35094 |
| Product | Medtronic Zinetics Manometric Catheter, Model 9012P2271. Water perfused, motility catheter. Distributed by Medtronic, Inc. 710 Medtronic Parkway NE, Minneapolis, MN 55432-5604 USA. |
| Product code | KLA |
| Recalling firm | Medtronic Gastroenterology / Urology |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jan 16, 2007 |
| FEI number | 1000135098 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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