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FDAAugust 8, 2018device

Bronchofibercope BF-6C240

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

The hazard

The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.

What to do

FDA enforcement status: Terminated

Brands named

olympus

Recall history

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

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