83 results
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37ms
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Sources: EU EUDAMED, US FDA
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FDA Recall
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Bronchial Double Lumen Tube Set (Left), Extra Length, Sterile
FDA Recall
Terminated
·Teleflex, Inc.·Product code BTS·November 21, 2014
RSCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal Tube is designated for oral or nasal intubation and are indicated for airway management. The product may be used to reduce the potential for kinking whenever an unusual positioning of the head or neck is required following intubation.
FDA Recall
Terminated
·Teleflex, Inc.·Product code BTR·December 12, 2014
Bronchial Double Lumen Tube Set (Right), Sterile
FDA Recall
Terminated
·Teleflex, Inc.·Product code BTS·November 21, 2014
Tracheopart Set (Right), Sterile
FDA Recall
Terminated
·Teleflex, Inc.·Product code BTS·November 21, 2014
Bronchial One Lumen Tube - Left
FDA Recall
Terminated
·Teleflex, Inc.·Product code BTS·November 21, 2014
Bronchial One Lumen Tube - Right
FDA Recall
Terminated
·Teleflex, Inc.·Product code BTS·November 21, 2014
Carlens Bronchial Double Lumen Tube Set (Left) Sterile
FDA Recall
Terminated
·Teleflex, Inc.·Product code BTS·November 21, 2014
Bronchial Double Lumen Tube Set (Left), Sterile
FDA Recall
Terminated
·Teleflex, Inc.·Product code BTS·November 21, 2014
White Bronchial Double Lumen Tube Set (Right) Sterile
FDA Recall
Terminated
·Teleflex, Inc.·Product code BTS·November 21, 2014
Tracheopart Set (Left), Sterile
FDA Recall
Terminated
·Teleflex, Inc.·Product code BTS·November 21, 2014
MAQUET Servo Humidifier 163; Model No.: 01-06-8125-8, catalog no. XKC01-06-8125-8. A heat and moisture condenser (artificial nose) is a device intended to be positioned over a tracheotomy (a surgically created opening in the throat) or tracheal tube (a tube inserted into the trachea) to warm and humidify gases breathed in by a patient.
FDA Recall
Terminated
·Teleflex, Inc.·Product code BYD·December 4, 2014
UroLift System REF UL400-4, QTY 4 Urolfit System with Handle Release Tool
FDA Recall
Open, Classified
·Neotract Inc·Product code PEW·June 24, 2022
Hudson RICA Sher-I-Swiv & Sher-I-Swiv F/O, Teleflex Medical, Research Triangle Park, NC 27709. Indicated for use in thoracic surgery, bronchospirometry, for the administration of endobronchial anesthesia and other uses commonly associated with endobronchial tubes.
FDA Recall
Terminated
·Teleflex Medical·Product code BZA·July 31, 2009
Hudson RICA Sheridan, Sher-I-Bronch Accessory Pack, Teleflex Medical, Research Triangle Park, NC 27709. Indicated for use in thoracic surgery, bronchospirometry, for the administration of endobronchial anesthesia and other uses commonly associated with endobronchial tubes.
FDA Recall
Terminated
·Teleflex Medical·Product code BZA·July 31, 2009
Hudson RICA Sheridan, EB Tube, Sher-I-Bronch, LS, 35FR, Nova Plus, 37FR, 39 FR, and 41 FR, Teleflex Medical, Research Triangle Park, NC 27709. Indicated for use in thoracic surgery, bronchospirometry, for the administration of endobronchial anesthesia and other uses commonly associated with endobronchial tubes.
FDA Recall
Terminated
·Teleflex Medical·Product code BZA·July 31, 2009
AquaPak Sterile Water for Inhalation, USP, 760 mL blow-molded plastic bottle for use with a respiratory gas humidifier; 10 bottles per case; manufactured by Hudson Respiratory Care, Inc., Temecula, CA 92589-9020 USA; catalog #037-00
FDA Recall
Terminated
·Teleflex Medical·Product code BTT·December 1, 2005
Hudson RICA Sheridan, ET Tube, Sher-I-Bronch RS, 28FR, 35 FR, 37 FR, 39FR and 41 FR, Teleflex Medical, Research Triangle Park, NC 27709. Indicated for use in thoracic surgery, bronchospirometry, for the administration of endobronchial anesthesia and other uses commonly associated with endobronchial tubes.
FDA Recall
Terminated
·Teleflex Medical·Product code BZA·July 31, 2009
Hudson RICA Sheridan, ET Tube, Sher-I-Bronch LS, 28FR, 35FR, 37FR, 39FR and 41FR, Teleflex Medical, Research Triangle Park, NC 27709. Indicated for use in thoracic surgery, bronchospirometry, for the administration of endobronchial anesthesia and other uses commonly associated with endobronchial tubes.
FDA Recall
Terminated
·Teleflex Medical·Product code BZA·July 31, 2009
Iso-Gard Filter S, Tethered Cap, REF: a) 19211T, OUS only; b) 19212T, OUS only; Microbial medical gas filter, single-use
FDA Recall
Open, Classified
·TELEFLEX LLC·Product code CAH·August 29, 2022
Iso-Gard Filter S, with Expandi-Flex, REF: a) 19261, OUS only; b) 19272, OUS only; Microbial medical gas filter, single-use
FDA Recall
Open, Classified
·TELEFLEX LLC·Product code CAH·August 29, 2022