Device recall
Z-1825-2023: Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020
FDA device recall · Class II · Remote Diagnostic Technologies Ltd.
Key facts
| Recall number (Z-number) | Z-1825-2023 |
|---|---|
| Recall event | 92251 |
| Product | Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 |
| Product code | LDD |
| Recalling firm | Remote Diagnostic Technologies Ltd. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K200849 |
| FEI number | 3003832357 |
At a glance
- 1–9 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