Device recall
Z-2212-2024: Product not distributed in the US. Implantable Cardioverter Defibrillators: a…
FDA device recall · Class II · Medtronic Inc.
Key facts
| Recall number (Z-number) | Z-2212-2024 |
|---|---|
| Recall event | 94674 |
| Product | Product not distributed in the US. Implantable Cardioverter Defibrillators: a. VIVA QUAD XT CRT-D, Model Number DTBA2QQ. b. CLARIA MRI CRT-D SureScan, Model Number DTMA2D1. c. CLARIA MRI QUAD CRT-D SureScan, Model Number DTMA2QQ. d. AMPLIA MRI CRT-D SureScan, Model Number DTMB2D1. e. AMPLIA MRI… |
| Product code | LWS |
| Recalling firm | Medtronic Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 2182208 |
At a glance
- None 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