FDADecember 9, 2022device

Luminos Agile Max, Luminos dRF Max, and LUMINOS Lotus Max

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

There is potential for the footrest to detach from the patient table during use. Device intended to visualize anatomical structures by converting an Xray pattern into a visible image. The system has medical applications ranging from gastrointestinal examinations to cranial, skeletal, thoracic and lung exposures as well as examinations of the urogenital tract. The unit may also be used in emergency applications, lymphography, endoscopy, myelography, venography, arthrography, interventional radiology, digital angiography, and digital subtraction angiography (DSA). The system may be used on pediatric, adult, and bariatric patients. These devices are not for mammography examinations.

What to do

FDA enforcement status: Ongoing

Brands named

siemens medical solutionssiemenssiemens medical

UPCs

40568690091622405686900915534056869269331

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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