FDAOctober 30, 2017device

VariCam

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

The hazard

A potential hazardous situation may occur if the collimator locking handle is not properly placed in the lock position and the warning circuit does not detect that the collimator is unlocked because of the patient proximity to the collimator during a clinical scan.

What to do

FDA enforcement status: Completed

Brands named

ge healthcare

UPCs

0000000010203000000001019100000310018290000812518180000000001015000000000106300008125165900000009940400000000010310000000001082000081251670000081251809

Recall history

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

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VariCam — Recall Details · AllClear