Device recall
Z-0805-05: LAERDAL ADAPTER CABLE, Cat. No. 920650. The cables allow the use of the Laerdal…
FDA device recall · Class I · Laerdal Medical Corporation
Key facts
| Recall number (Z-number) | Z-0805-05 |
|---|---|
| Recall event | 31571 |
| Product | LAERDAL ADAPTER CABLE, Cat. No. 920650. The cables allow the use of the Laerdal HeartStart multifunction defibrillator pads to be used with the HeartStart 3000 and 4000 series defibrillators and Philips Medical Systems CodeMaster 100 and XL series defibrillators. The Adapter Cable is supplied to… |
| Product code | LDD |
| Recalling firm | Laerdal Medical Corporation |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jan 18, 2008 |
| FEI number | 2425852 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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