Philips Medical Systems is recalling 619 units of ceiling suspension telescopic carriages used in various diagnostic imaging systems. These carriages, manufactured between July 2024 and June 2025, have potential manufacturing issues that make them difficult to move vertically. This defect requires healthcare operators to use additional force or physical exertion to manually move the equipment during medical procedures. The recall affects several systems, including the ProxiDiagnost N90, CombiDiagnost R90, Precision CRF, DigitalDiagnost 4, DigitalDiagnost C90, and Radiography 7300 C. Philips is initiating this voluntary recall to address the physical exertion risk to clinicians and technicians.
The telescopic carriage may become stuck or difficult to move up and down, requiring excessive physical force from the operator. This poses a risk of physical strain or injury to the medical professional and could potentially cause delays or positioning difficulties during diagnostic imaging.
Recall #: Z-0461-2026
Recall #: Z-0462-2026
Recall #: Z-0463-2026
Recall #: Z-0464-2026
Recall #: Z-0465-2026
Recall #: Z-0466-2026
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.
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Sources: FDA iRES · Raw API Response
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