Medical Device Recalls
-
21 to 27 of 27 Results
510(K) Number: K822082 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
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 Nasal Tracheal Tube, 7.5 mm; a Rx, sterile, single use tracheal tube; Huds... | 3 | 11/02/2006 | 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 |
Novaplus Sheridan/HVT Cuffed, Murphy Eye Tracheal Tube; an Rx, ETO sterilized, single use device ins... | 3 | 03/10/2005 | Teleflex Medical |
Sheridan Endotracheal Tube contained inside Centurion kit code TC7855. | 1 | 07/30/2019 | Centurion Medical Products Corporation |
-