Drug recall
Philips MX 16-Slice CT Scanner System, a whole-body computed tomography X-ray system.
FDA recall event 64389 · Class II · Philips Medical Systems (Cleveland) Inc
Key facts
| Event ID | 64389 |
|---|---|
| Recall numbers | Z-0899-2013 |
| Recalling firm | Philips Medical Systems (Cleveland) Inc |
| Product type | Devices |
| Products | Philips MX 16-Slice CT Scanner System, a whole-body computed tomography X-ray system. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The four screws that secure the patient table top to the carrier became loose, which caused the table top to detach. |
| Initiation date | Dec 19, 2012 |
| Report date | Mar 6, 2013 |
| Termination date | Dec 3, 2013 |
| City | Cleveland |
| State | OH |
| Country | United States |
| FEI number | 1525965 |
At a glance
- 1–9 Products in this recall
- 10–99 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: