Device recall
Z-0598-05: Medtronic Maximo VR, model 7232 Single Chamber Implantable Cardioverter…
FDA device recall · Class II · Medtronic Inc. Cardiac Rhythm Managment
Key facts
| Recall number (Z-number) | Z-0598-05 |
|---|---|
| Recall event | 31142 |
| Product | Medtronic Maximo VR, model 7232 Single Chamber Implantable Cardioverter Defibrillator (ICD)devices are tiered therapy implantable arrhythmia control devices, which provide automatic detection of ventricular arrhythmias and delivery of user-selected therapies for the detected arrhythmia. Therapies… |
| Product code | LWS |
| Recalling firm | Medtronic Inc. Cardiac Rhythm Managment |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 28, 2006 |
| PMA numbers | P980016, P980016S037 |
| FEI number | 2182208 |
At a glance
- None Linked 510(k)s
- 1–9 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