Medical Device Recalls
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21 to 27 of 27 Results
510(K) Number: K822082 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Hudson RCI Sheridan/HVT: a) 5.0 mm, REF 5-10310 b) 5.5 mm, REF 5-10311 c) 6.0 mm, REF 5-10312 d)... | 1 | 09/09/2019 | Teleflex Medical |
Hudson RCI Sheridan/CF: a) 3.0 mm, REF 5-10106, REF 5-10206 b) 3.5 mm, REF 5-10107 c) 4.0 mm, RE... | 1 | 09/09/2019 | Teleflex Medical |
Hudson RCI Sheridan Uncuffed: a) 2.0 mm, REF 5-10404 b) 2.5 mm, REF 5-10405 c) 3.0 mm, REF 5-10... | 1 | 09/09/2019 | Teleflex Medical |
Hudson RCI Sheridan Preformed: a) 3.0 mm, REF 5-22006, REF 5-22106 b) 3.5 mm, REF 5-22007, REF 5-2... | 1 | 09/09/2019 | Teleflex Medical |
Hudson RCI Sheridan LTS: a) 4.0 mm, REF 5-11108 b) 5.0 mm, REF 5-11110 c) 6.0 mm, REF 5-11112 ... | 1 | 09/09/2019 | Teleflex Medical |
Hudson RCI Sheridan LTS, Product Code 5-11112 Product Usage: Tracheal tube/airway management | 1 | 06/19/2019 | Teleflex Medical |
Hudson RCI Sheridan EZ-ENDO: a) 5.0 mm, REF 5-22510 b) 5.5 mm, REF 5-22511 c) 7.0 mm, REF 5-22514... | 1 | 09/09/2019 | Teleflex Medical |
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