Device recall
Z-1616-2008: 9051 Electrode Adapter; Automated external defibrillator, Used with QUIK-COMBO…
FDA device recall · Class III · Cardiac Science Corporation
Key facts
| Recall number (Z-number) | Z-1616-2008 |
|---|---|
| Recall event | 47205 |
| Product | 9051 Electrode Adapter; Automated external defibrillator, Used with QUIK-COMBO System; Cardiac Science Corp, Bothell, WA 98021. |
| Product code | MKJ |
| Recalling firm | Cardiac Science Corporation |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 21, 2011 |
| 510(k) numbers | K971149 |
| 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