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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 28 of 28 Results
510(K) Number: K780900
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Product Description
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Recall
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RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480035 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150020 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150025 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150030 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150035 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150040 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal. Intended for patients requiring ... 2 01/23/2023 FEI # 3005747797
TELEFLEX LLC
RUSCH Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF numbers: a) 170050 b) 170... 2 08/19/2021 FEI # 3007134520
Teleflex Medical Europe Ltd
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