Philips Medical Systems Nederland B.V. is recalling approximately 4,596 AD7 and AD7X patient tables used with Allura and Azurion medical imaging systems. During manual repositioning of the tabletop, a finger can become caught between the guiding rails and the table surface. No injuries have been reported to date, but the defect poses a risk of crushing or pinching injuries to healthcare operators and service personnel. Users are advised to stop using the affected tables and contact Philips for equipment correction or replacement.
A finger can become entrapped between the longitudinal guiding rails and the tabletop during manual movement. This mechanism can cause physical injury to the person adjusting the equipment.
Recall #: Z-1076-2025; Quantity: 119 units OUS
Recall #: Z-1077-2025; Quantity: 474 units US, 1908 units OUS
Recall #: Z-1078-2025; Quantity: 146 units US, 629 units OUS
Recall #: Z-1079-2025; Quantity: 1 unit OUS
Recall #: Z-1080-2025; Quantity: 1528 units US, 3482 units OUS
Recall #: Z-1081-2025; Quantity: 66 units US, 79 units OUS
Recall #: Z-1082-2025; Quantity: 1 unit OUS
Recall #: Z-1083-2025; Quantity: 1 unit US, 1 unit OUS
Recall #: Z-1084-2025; Quantity: 22 units US, 65 units OUS
Recall #: Z-1085-2025; Quantity: 33 units US, 82 units OUS
Recall #: Z-1086-2025; Quantity: 69 units US, 235 units OUS
Recall #: Z-1087-2025; Quantity: 9 units US, 101 units OUS
Recall #: Z-1088-2025; Quantity: 42 units US, 661 units OUS
Recall #: Z-1089-2025; Quantity: 6 units US, 246 units OUS
Recall #: Z-1090-2025; Quantity: 68 units US, 438 units OUS
Recall #: Z-1091-2025; Quantity: 90 units US, 458 units OUS
Recall #: Z-1092-2025; Quantity: 251 units US, 938 units OUS
Recall #: Z-1093-2025; Quantity: 324 units US, 1390 units OUS
Recall #: Z-1094-2025; Quantity: 1346 units US, 2582 units OUS
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
openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.