Maquet Datascope Corp: 6 recalls on record

Recalls filed with 1 agency: FDA (6).

First recall on record: May 28, 2014. Most recent: November 7, 2018.

Risk classification: Class I: 6

Most recent recalls

DateAgencyProduct
November 7, 2018FDACardiosave Rescue IABP, Part Number 0998-UC-0800-83Z-0100-2019
September 13, 2017FDACS 100 Intra-Aortic Balloon Pump. It supports the heart's left ventricle by increasing…Z-3086-2017
August 2, 2017FDACS 100 Intra-Aortic Balloon PumpZ-2737-2017
August 2, 2017FDACS 300 Intra-Aortic Balloon PumpZ-2738-2017
August 2, 2017FDACS 100i Intra-Aortic Balloon PumpZ-2736-2017
May 28, 2014FDADatascope System 98/98xt, CS 100/CS100i and CS 300 Intra-Aortic Balloon Pump. The Int…Z-1523-2014

Questions about this company

How many recalls does Maquet Datascope Corp have?
Recalert has 6 U.S. recalls on record for Maquet Datascope Corp, published between May 28, 2014 and November 7, 2018.
What was the most recent Maquet Datascope Corp recall?
FDA recall Z-0100-2019, published November 7, 2018: Cardiosave Rescue IABP, Part Number 0998-UC-0800-83
Which agencies have handled Maquet Datascope Corp recalls?
Maquet Datascope Corp appears as the recalling firm in recalls from: FDA (6).

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