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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K161359
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Product Description
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Recall
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FDA Recall
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AC/DC POWER SUPPLY for 7400, Part Number 151004300, XP Power Model Number AHM180PS19-XE0338, AC/DC A... 2 09/30/2020 FEI # 3014563045
ESAOTE S.P.A
AC/DC POWER SUPPLY for 7400, Part Number 151004301, XP Power Model Number AHM180PS19-XE1057, AC/DC A... 2 09/30/2020 FEI # 3014563045
ESAOTE S.P.A
MyLab Alpha, Model 7400 2 10/23/2018 FEI # 3012981490
ESAOTE S.P.A.
MyLab Gamma, Model 7410 2 10/23/2018 FEI # 3012981490
ESAOTE S.P.A.
MyLab Seven, Model 6400 2 10/23/2018 FEI # 3012981490
ESAOTE S.P.A.
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