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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 9 of 9 Results
510(K) Number: K931166
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180030 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180035 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180040 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180045 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180070 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180055 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180060 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180065 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180050 1 06/29/2023 FEI # 3005747797
TELEFLEX LLC
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