FDAJune 21, 2016device

Ingenuity Flex, model # 728317; Intended to produce cross- sectional images of the body.

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

The hazard

Supplier design change contributed to a thinner plastic which was used as part of the cover on the devices. The thinner plastic cover may crack causing injury to patients, operators, by-standers and service personnel.

What to do

FDA enforcement status: Terminated

Brands named

philips medical systems clevelandphilipsphilips medical

Recall history

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

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