Device recall
Z-0523-2008: life+cel, Replacement Battery for Cardiac Science Powerheart AED G3, Lithium…
FDA device recall · Class II · BatteryZone, Inc.
Key facts
| Recall number (Z-number) | Z-0523-2008 |
|---|---|
| Recall event | 45814 |
| Product | life+cel, Replacement Battery for Cardiac Science Powerheart AED G3, Lithium Sulfur Dioxide, OEM P/N: 9146-001, voltage 12V, 7.5 amps, Mfg for Battery Zone, Inc ; Mfg by Nordix, Inc. |
| Product code | MKJ |
| Recalling firm | BatteryZone, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 1, 2013 |
| FEI number | 3006525760 |
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