Device recall
Z-1782-2010: ReviveR AED semiautomatic external defibrillator used with the DBP-2800 Battery…
FDA device recall · Class I · Defibtech LLC
Key facts
| Recall number (Z-number) | Z-1782-2010 |
|---|---|
| Recall event | 55497 |
| Product | ReviveR AED semiautomatic external defibrillator used with the DBP-2800 Battery Pack. Manufactured by Defibtech, LLC. Seymour, CT 06483. The DBP-2800 battery pack is an accessory to the AED and does not have its own intended use. The AED is intended for use on victims of sudden cardiac arrest when… |
| Product code | MKJ |
| Recalling firm | Defibtech LLC |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Sep 29, 2020 |
| 510(k) numbers | K013896 |
| FEI number | 3006403206 |
At a glance
- 1–9 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