Device recall
Z-1938-2019: Powerheart G5 Automatic AED
FDA device recall · Class II · Cardiac Science Corporation
Key facts
| Recall number (Z-number) | Z-1938-2019 |
|---|---|
| Recall event | 83103 |
| Product | Powerheart G5 Automatic AED |
| Product code | MKJ |
| Recalling firm | Cardiac Science Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 15, 2021 |
| PMA numbers | P160033 |
| FEI number | 2112020 |
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