Drug recall
ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027;
FDA recall event 98434 · Class II · PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Key facts
| Event ID | 98434 |
|---|---|
| Recall numbers | Z-1659-2026, Z-1660-2026, Z-1661-2026, Z-1662-2026, Z-1663-2026, Z-1664-2026, Z-1665-2026, Z-1666-2026, Z-1667-2026, Z-1668-2026, Z-1669-2026, Z-1670-2026 and 10 more |
| Recalling firm | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Product type | Devices |
| Products | ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027;, Allura Xper FD10C; System Code: 722001;, ALLURA Xper FD10F; System Code: 722002;, ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033;, ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026; and 17 more |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. |
| Initiation date | Mar 3, 2026 |
| Report date | Apr 8, 2026 |
| City | Best |
| Country | Netherlands |
| FEI number | 3042175844 |
At a glance
- 10–99 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: