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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
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-0035-2022 - CardioQuip, Modular Cooler-Heater, Model: MCH-1000(i), CE 2797, UDI: (01)00860000846103 2 10/06/2021 CardioQuip, LLC
Z-0038-2022 - CardioQuip, Modular Cooler-Heater 1000(m),Thermoelectric Cooling Lid, Model: MCH-11TEC,CE 2797, UDI: (01) 00860000846134 2 10/06/2021 CardioQuip, LLC
Z-0037-2022 - CardioQuip, Modular Cooler-Heater 1000(m),Compact Unit, Model:MCH-1000(m),CE 2797, UDI: (01)00860000846110 2 10/06/2021 CardioQuip, LLC
Z-0036-2022 - CardioQuip, Modular Cooler-Heater 1000(i), Standard Unit, Model: MCH-10RMS, CE 2797, UDI: (01) 00860000846127 2 10/06/2021 CardioQuip, LLC
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