Drug recall
Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, and 00-1007…
FDA recall event 92914 · Class II · Remote Diagnostic Technologies Ltd.
Key facts
| Event ID | 92914 |
|---|---|
| Recall numbers | Z-2625-2023 |
| 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, and 00-1007, when Used With Tempus Pro Video Laryngoscope, REF 01-2044 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Full screen error message may occur on patient monitors with affected hardware version, either during or after laryngoscopes are unplugged from monitors, informing users a 60-100 second… |
| Initiation date | Aug 24, 2023 |
| Report date | Sep 27, 2023 |
| 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: