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Recall Observatory FDA recall evidence

Device product

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

Z-1002-2023

December 09, 2022

Class II

Product summary

Firm
Siemens Medical Solutions USA, Inc
Event
Event 91383
Status
Ongoing
Classification
Class II
Quantity
886 units
Official record key
device-enforcement:Z-1002-2023

Official wording

Reason: 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.

Code information: All serial numbers 1) Luminos Agile Max, Material #10762472, UDI/DI: 4056869009162 2) Luminos drF Max, Material #10762471, UDI/DI: 4056869009155 3) Luminos Lotus Max, Material #11574100, UDI/DI: 4056869269331

Distribution pattern: Worldwide distribution

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.