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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K122253
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Product Description
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Recall
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FDA Recall
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HGE Healthcare Patient Monitor B30, Procare Monitor B20, Procare Monitor B40, and Monitor B40 K1222... 2 12/12/2013 FEI # 2126677
GE Healthcare, LLC
PROCARE B20 Patient Monitor, V1; and B20 Patient Monitor, V2. The PROCARE Monitor B20 is a portab... 2 12/07/2018 FEI # 2126677
GE Healthcare, LLC
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