FDAJuly 2, 2025device

GE HealthCare OEC 9800.

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

The hazard

GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in certain OEC 9800 and OEC 9900 Elite C-arm Systems. Specifically, impacted systems are missing the full layer of lead tape in the collimator covers, which will lead to a small increase in radiation exposure to the patient and/or operator. The missing lead tape is not detectable by the user.

What to do

FDA enforcement status: Ongoing

Brands named

ge medical systems

UPCs

00840682114349

Recall history

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

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