FDAJune 1, 2015device

HUDSON RCI, Sheridan, SHER-I-SWIV and SHER-I-SWIV/FO Double Swivel, Rx Only, Sterile. Used temporarily to make rigid a flexible tracheal tube to aid its insertion into a patient.

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

The hazard

The double swivel connector may crack or separate on the endobronchial tube.

What to do

FDA enforcement status: Terminated

Brands named

teleflex medicalteleflex

Recall history

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

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