Philips Medical Systems is recalling 4,234 Allura Xper medical imaging systems because internal parts like batteries, hard drives, and power supplies can wear out and fail. If these components deteriorate, the system's motorized movements—which are used to position the equipment around a patient—may stop working during a procedure. While automated movements might fail, manual movements of the stand and table remain functional, and the X-ray imaging capabilities are not affected. Philips has initiated this voluntary recall to address the deterioration of these internal components.
A failure of motorized movements during a medical procedure can prevent the precise positioning of imaging equipment, potentially leading to delays in treatment or the need to manually reposition the system. While manual overrides are available, a sudden loss of automated control could complicate time-sensitive medical interventions.
Quantity: 1117 units (252 US, 865 OUS). Recall #: Z-2623-2025.
Quantity: 286 units (67 US, 219 OUS). Recall #: Z-2624-2025.
Quantity: 2 units (1 US, 1 OUS). Recall #: Z-2625-2025.
Quantity: 2114 units (791 US, 1323 OUS). Recall #: Z-2626-2025.
Quantity: 268 units (102 US, 166 OUS). Recall #: Z-2627-2025.
Quantity: 174 units (45 US, 129 OUS). Recall #: Z-2628-2025.
Quantity: 5 units (2 US, 3 OUS). Recall #: Z-2629-2025.
Quantity: 75 units (26 US, 49 OUS). Recall #: Z-2630-2025.
Quantity: 3 units (OUS only). Recall #: Z-2631-2025.
Quantity: 45 units (11 US, 34 OUS). Recall #: Z-2632-2025.
Quantity: 98 units (23 US, 75 OUS). Recall #: Z-2633-2025.
Quantity: 1 units (OUS only). Recall #: Z-2634-2025.
Quantity: 46 units (OUS only). Recall #: Z-2635-2025.
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response
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