Drug recall
Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, 00-1007
FDA recall event 96719 · Class II · Remote Diagnostic Technologies Ltd.
Key facts
| Event ID | 96719 |
|---|---|
| Recall numbers | Z-1729-2025 |
| Recalling firm | Remote Diagnostic Technologies Ltd. |
| Product type | Devices |
| Products | Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, 00-1007 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Patient Monitor software update to address issues:1)May freeze at startup with MPM Application error and Attention Restart Required messages,2)Monitor may freeze and reboot at start of 12-lead ECG or… |
| Initiation date | Apr 15, 2025 |
| Report date | May 14, 2025 |
| City | Farnborough |
| Country | United Kingdom |
| FEI number | 3003832357 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: