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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K800742
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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CAIRE Liberator 45, MODEL 13261699, Liquid Oxygen System Unit 1 12/02/2022 Caire, Inc.
CAIRE Liberator 20, MODEL 13256195, Liquid Oxygen System Unit 1 12/02/2022 Caire, Inc.
CAIRE Liberator 30, MODEL 13337403, Liquid Oxygen System Unit 1 12/02/2022 Caire, Inc.
CAIRE Liberator 45, MODEL 13262253, Liquid Oxygen System Unit 1 12/02/2022 Caire, Inc.
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