Recall Z-1429-2017 — Apollo DRF; Model: 9784220831 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures
U.S. FDA — Device Enforcement · Italy · 2016-12-27 · Class II
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Reported risk: Patient fell from the table because the footrest of the device detached from the table top while the patient was positioned on the table and table was moving from vertical position.
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