FDAFebruary 18, 2021device

RUSCH¿ POLARIS" Laryngoscope - Product Usage: intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.

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

The hazard

Teleflex is voluntarily recalling the products referenced above due to customers reporting that the laryngoscope handles develop cracks and/or break at the hinge.

What to do

FDA enforcement status: Ongoing

Brands named

teleflex medicalteleflex

UPCs

140267046625522402670466255934026704662556140267046625692402670466256634026704662563140267046625762402670466257334026704662570

Recall history

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

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