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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K123125
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Product Description
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FDA Recall
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GE Healthcare, Avance, Avance CS2, Aisys, Aespire View, and Engstrom. Intended for volume or pres... 1 10/15/2013 GE Healthcare, LLC
GE Healthcare, Aisys, Amingo, Avance, and Avance CS2. Intended for volume or pressure control ven... 1 10/15/2013 GE Healthcare, LLC
Canister: CO2 canister with GE part numbers 1407-3200-000, 1407-7004-000, or M1084850. Intended ... 2 06/03/2013 GE Healthcare, LLC
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