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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 12 Results
510(K) Number: K931163
 
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Product Description
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Recall
Class
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FDA Recall
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Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780035 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780040 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780045 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780050 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780055 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780090 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780065 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780070 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780075 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780080 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
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