Drug recall
Spectral CT 7500, Software Version 5.0.0.X. Computed Tomography X-Ray System.
FDA recall event 93640 · Class II · Philips North America Llc
Key facts
| Event ID | 93640 |
|---|---|
| Recall numbers | Z-0725-2024 |
| Recalling firm | Philips North America Llc |
| Product type | Devices |
| Products | Spectral CT 7500, Software Version 5.0.0.X. Computed Tomography X-Ray System. |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Multiple software issues that affect device functionality. |
| Initiation date | Nov 30, 2023 |
| Report date | Jan 24, 2024 |
| City | Cambridge |
| State | MA |
| Country | United States |
| FEI number | 3016618143 |
At a glance
- 1–9 Products in this recall
- None 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: