Drug recall
Incisive CT Computed Tomography X-ray System Model: 728143
FDA recall event 87427 · Class II · Philips North America Llc
Key facts
| Event ID | 87427 |
|---|---|
| Recall numbers | Z-1265-2021 |
| Recalling firm | Philips North America Llc |
| Product type | Devices |
| Products | Incisive CT Computed Tomography X-ray System Model: 728143 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Actuators in the Incisive gantry could result in the gantry failure to self-lock if both of the 2 sides actuators fail. In some cases in systems with affected components, the gantry may tilt forward… |
| Initiation date | Feb 22, 2021 |
| Report date | Mar 24, 2021 |
| Termination date | Feb 9, 2023 |
| 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: