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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 28 Results
510(K) Number: K780900
 
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Product Description
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Recall
Class
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FDA Recall
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Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170050 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150055 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170055 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170060 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170065 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170070 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170075 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170080 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170085 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170090 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
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