Device recall
Z-1121-2014: Medtronic Everest 20cc Inflation Device; Model Number and Catalog Number…
FDA device recall · Class III · Medtronic Vascular
Key facts
| Recall number (Z-number) | Z-1121-2014 |
|---|---|
| Recall event | 67490 |
| Product | Medtronic Everest 20cc Inflation Device; Model Number and Catalog Number: AC2205P The Everest 20cc Inflation device is designed to be used to inflate / deflate balloon catheters as well as to monitor pressure within the balloon. The Everest 20atm Device is outfitted with a manometer with measuring… |
| Product code | MAV |
| Recalling firm | Medtronic Vascular |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jun 2, 2014 |
| 510(k) numbers | K942269 |
| FEI number | 1220452 |
At a glance
- 1–9 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