Device recall
Z-1108-05: VITALITY AVT, model A135 and A155. Implantable Cardioverter Defibrillator…
FDA device recall · Class I · Boston Scientific CRM Corp
Key facts
| Recall number (Z-number) | Z-1108-05 |
|---|---|
| Recall event | 32738 |
| Product | VITALITY AVT, model A135 and A155. Implantable Cardioverter Defibrillator. Atrial and Ventricular Therapies. Sterilized using gaseous ethylene oxide. Guidant Corporation Caridac Rhythm Managment, 4100 Hamline Avenue North, St. Paul, MN 55112-5798, USA. |
| Product code | LWP |
| Recalling firm | Boston Scientific CRM Corp |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Apr 7, 2008 |
| PMA numbers | P960040, P960040S035, P960040/S29 |
| FEI number | 2124215 |
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