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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 28 Results
510(K) Number: K780900
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Product Description
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Recall
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FDA Recall
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Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170095 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170120 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170125 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170130 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170135 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170140 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170145 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170150 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170155 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 1700100 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
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