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www.fdanews.com/articles/172813-teleflex-recalls-endobronchial-tube-due-to-faulty-connector

Teleflex Recalls Endobronchial Tube Due to Faulty Connector

August 27, 2015

Teleflex Medical has recalled 62,882 units of its Hudson RCI Sher-I-Bronch endobronchial tube because the double swivel connector may break or separate on the tube while it is inserted into a patient’s airways.

When breakage or separation occurs, the tube can leak, causing patients be deprived of oxygen. The Class I recall followed customer complaints.

The recall — involving 12 product codes — covers devices manufactured from October 2013 to April 2015 and distributed through May of this year. — Michael Cipriano