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Teleflex, Inc. Recalls

8 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Teleflex, Inc..

8Total Recalls
1Critical
2.3MUnits Affected
Dec 12, 2014Most Recent
All Recalls

Every Teleflex, Inc. Recall

Sorted by most recent. Click any recall for full details.

8 recalls
High RiskFDA
Teleflex, Inc.
R¿SCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal Tube is designated for oral or nasal intubation and are indicate...
Medical Devices·2,292,361 affected·Dec 12, 2014
CriticalFDA
Teleflex, Inc.
MAQUET Servo Humidifier 163; Model No.: 01-06-8125-8, catalog no. XKC01-06-8125-8. A heat and moisture condenser (artificial nose) is ...
Surgical Devices·18 affected·Dec 4, 2014
High RiskFDA
Teleflex, Inc.
Carlens Bronchial Double Lumen Tube Set (Left) Sterile
Medical Devices·0 affected·Nov 21, 2014
High RiskFDA
Teleflex, Inc.
Bronchial Double Lumen Tube Set (Right), Sterile
Medical Devices·0 affected·Nov 21, 2014
High RiskFDA
Teleflex, Inc.
Bronchial One Lumen Tube - Left
Medical Devices·0 affected·Nov 21, 2014
High RiskFDA
Teleflex, Inc.
Bronchial Double Lumen Tube Set (Left), Sterile
Medical Devices·6,991 affected·Nov 21, 2014
High RiskFDA
Teleflex, Inc.
Bronchial One Lumen Tube - Right
Medical Devices·0 affected·Nov 21, 2014
High RiskFDA
Teleflex, Inc.
Tracheopart Set (Right), Sterile
Medical Devices·0 affected·Nov 21, 2014