FDADecember 27, 2016device

Apollo EZ; Model: 9784152036 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures

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

The hazard

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.

What to do

FDA enforcement status: Terminated

Brands named

villa sistemi medicali s p avillavilla sistemi

Recall history

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

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