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U.S. Department of Health and Human Services

Medical Device Recalls

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21 to 27 of 27 Results
510(K) Number: K822082
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Product Description
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FDA Recall
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Sheridan/CF Cuffed Tracheal Tube, Sterile, Rx only, Teleflex Medical, Research Triangle Park, NC 277... 2 12/12/2014 Teleflex Medical
Sheridan Preformed Cuffed Tracheal Tube, Nasal 7.0, Catalog Number: 5-22314, Teleflex Medical Ltd, R... 2 08/26/2009 Teleflex Medical
Sheridan Preformed Cuffed Tracheal Tube, Nasal 6.5, Catalog Number: 5-22313, Teleflex Medical Ltd, R... 2 08/26/2009 Teleflex Medical
Sheridan Preformed Cuffed Oral Tracheal Tube, 5.0 mm; a Rx, sterile, single use tracheal tube; Hudso... 3 11/02/2006 Teleflex Medical
Sheridan Preformed Uncuffed Oral Tracheal Tube, 3.0 mm; a Rx, sterile, single use tracheal tube; Hud... 3 11/02/2006 Teleflex Medical
Sheridan Preformed Cuffed Nasal Tracheal Tube, 7.5 mm; a Rx, sterile, single use tracheal tube; Huds... 3 11/02/2006 Teleflex Medical
Novaplus Sheridan/HVT Cuffed, Murphy Eye Tracheal Tube; an Rx, ETO sterilized, single use device ins... 3 03/10/2005 Teleflex Medical
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