Drug recall
Philips Allura Xper System: Interventional Fluoroscopic X-Ray System Product No.: 722026, 722027, 722028…
FDA recall event 87978 · Class II · Philips Medical Systems Nederlands
Key facts
| Event ID | 87978 |
|---|---|
| Recall numbers | Z-1904-2021 |
| Recalling firm | Philips Medical Systems Nederlands |
| Product type | Devices |
| Products | Philips Allura Xper System: Interventional Fluoroscopic X-Ray System Product No.: 722026, 722027, 722028, 722029, 722035, 722038, and 722058. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Certain low-voltage DC power supplies (DCPS) used in these products may be subject to an increased probability of failure. Failure of a DCPS may result in the sudden loss of imaging functionality or… |
| Initiation date | Jun 23, 2016 |
| Report date | Jun 30, 2021 |
| Termination date | Feb 8, 2023 |
| City | Best |
| Country | Netherlands |
| FEI number | 3003768277 |
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: