Teleflex, Inc.: 5 recalls on record

Recalls filed with 1 agency: FDA (5).

First recall on record: February 18, 2015. Most recent: August 26, 2015.

Risk classification: Class I: 1 · Class II: 4

Most recent recalls

DateAgencyProduct
August 26, 2015FDACarlens Bronchial Double Lumen Tube Set (Left) SterileZ-2411-2015
August 26, 2015FDABronchial One Lumen Tube - LeftZ-2409-2015
August 26, 2015FDABronchial Double Lumen Tube Set (Right), SterileZ-2408-2015
February 25, 2015FDAR¿SCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal Tube is designat…Z-1124-2015
February 18, 2015FDAMAQUET Servo Humidifier 163; Model No.: 01-06-8125-8, catalog no. XKC01-06-8125-8. A h…Z-1008-2015

Questions about this company

How many recalls does Teleflex, Inc. have?
Recalert has 5 U.S. recalls on record for Teleflex, Inc., published between February 18, 2015 and August 26, 2015.
What was the most recent Teleflex, Inc. recall?
FDA recall Z-2411-2015, published August 26, 2015: Carlens Bronchial Double Lumen Tube Set (Left) Sterile
Which agencies have handled Teleflex, Inc. recalls?
Teleflex, Inc. appears as the recalling firm in recalls from: FDA (5).

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