Atlas FDA

Teleflex, Inc.

11 FDA 510(k) clearances · Recalling firm

Sort:Newest firstOldest first

◉ Watch Teleflex, Inc.

RecordFirmDate
Bronchial Double Lumen Tube Set (Left), Sterile recall (Z-2407-2015)Teleflex, Inc.2015-08-18
Bronchial Double Lumen Tube Set (Right), Sterile recall (Z-2408-2015)Teleflex, Inc.2015-08-18
Bronchial One Lumen Tube - Left recall (Z-2409-2015)Teleflex, Inc.2015-08-18
Bronchial One Lumen Tube - Right recall (Z-2410-2015)Teleflex, Inc.2015-08-18
Carlens Bronchial Double Lumen Tube Set (Left) Sterile recall (Z-2411-2015)Teleflex, Inc.2015-08-18
Tracheopart Set (Left), Sterile recall (Z-2412-2015)Teleflex, Inc.2015-08-18
Tracheopart Set (Right), Sterile recall (Z-2413-2015)Teleflex, Inc.2015-08-18
White Bronchial Double Lumen Tube Set (Right) Sterile recall (Z-2414-2015)Teleflex, Inc.2015-08-18
Bronchial Double Lumen Tube Set (Left), Extra Length, Sterile recall (Z-2415-2015)Teleflex, Inc.2015-08-18
RSCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal Tube is designated recall (Z-1124-2015)Teleflex, Inc.2015-02-17
MAQUET Servo Humidifier 163; Model No.: 01-06-8125-8, catalog no. XKC01-06-8125-8. A heat recall (Z-1008-2015)Teleflex, Inc.2015-02-06

Track Teleflex, Inc. automatically

Every clearance here is in the API, with alerts when new ones post.