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FDAJune 21, 2016device

Brilliance CT Big Bore Oncology, model #728243; 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 and cause injury to patients, operators, by standers or 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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Brilliance CT Big Bore Oncology, model #728243; Intended to produce cross- sectional images of the body. — Recall Details · AllClear