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Latest Breaking News On - Cardiosave liion - Page 1 : comparemela.com
FDA Class I Recall of CardioSave Hybrid/Rescue IABPs
Subpar batteries that do not meet performance specifications were mistakenly released to a limited number of customers and may have a shortened run-time and fail unexpectedly.
United states
Datascope getinge maquet
Drug administration
Cardiosave hybrid
Cardiosave liion
Heart failure
Intra aortic balloon pump iabp
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