Device recall
Z-0990-04: Power Heart AED G3 Automated External Defibrillator IntelliSense (Lithium)…
FDA device recall · Class II · Cardiac Science, Inc.
Key facts
| Recall number (Z-number) | Z-0990-04 |
|---|---|
| Recall event | 29026 |
| Product | Power Heart AED G3 Automated External Defibrillator IntelliSense (Lithium) Battery, Model 9142 |
| Product code | MKJ |
| Recalling firm | Cardiac Science, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 18, 2005 |
| 510(k) numbers | K031987 |
| FEI number | 2112020 |
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