Drug recall
Philips Healthcare System X-ray Tomography Computed:
FDA recall event 75551 · Class II · Philips Electronics North America Corporation
Key facts
| Event ID | 75551 |
|---|---|
| Recall numbers | Z-0375-2017, Z-0376-2017 |
| Recalling firm | Philips Electronics North America Corporation |
| Product type | Devices |
| Products | Philips Healthcare System X-ray Tomography Computed : |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | FDA Requested |
| Reason for recall | It was discovered the patient support tabletop may fail to move in the horizontal direction when it is commanded to do so during CT scans due to a potential mechanical linkage failure. |
| Initiation date | Mar 15, 2016 |
| Report date | Nov 30, 2016 |
| Termination date | Sep 9, 2020 |
| City | Andover |
| State | MA |
| Country | United States |
| FEI number | 1218950 |
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: