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The United States Food and Drug Administration (FDA) provides updated information on our ongoing evaluation and monitoring of device failures associated with Getinge's Maquet / Datascope intra-aortic balloon pump (IABP) devices, including the Cardiosave (hybrid and rescue), CS300 and CS100 / CS100i. Datascope Accutorr Plus User Manual Accutorr Plus™ Operating Instructions 0070-10-0428-02 v Foreword Introduction Foreword This operating instructions is intended to provide information for the proper operation of the Datascope Accutorr Plus. fiber-optic IAB catheter; CS300 with Maquet datascope recalls intra-aortic balloon June 15, 2011 The U.S. Food and Drug Administration (FDA) said Maquet Datascope Corp. has issued a class I recall for its System 98/98XT, CS100/CS100i and CS300 . Each model is available with either Sealed Lead Acid or Lithium Ion Battery technology. 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