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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 15 of 15 Results
510(K) Number: K200107
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Product Description
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FDA Recall
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epoc BGEM Test Card (BUN & TCO2),Veterinary with epoc Host SW v3.37.3, epoc NXS SW v4.10.6, Sensor C... 2 08/28/2023 Siemens Healthcare Diagnostics Inc
epoc BGEM Crea Test Card with epoc Host SW v3.37.3, epoc NXS SW v4.10.6, Sensor Configuration 41.1 2 08/28/2023 Siemens Healthcare Diagnostics Inc
epoc BGEM BUN Test Card with epoc Host SW v3.37.3, epoc NXS SW v4.10.6, Sensor Configuration 41.1 2 08/28/2023 Siemens Healthcare Diagnostics Inc
epoc Host 2 as follows: Product SMN epoc NXS Host, US 11413475 epoc NXS Host, ... 2 03/03/2023 Siemens Healthcare Diagnostics Inc
Siemens epoc BGEM Test Card-In vitro diagnostic device for the quantitative testing of samples of he... 2 09/15/2020 Siemens Healthcare Diagnostics Inc
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