Datascope Corp. recalls

12 recalls on record · latest: February 6, 2026

Official U.S. recall history for Datascope Corp., compiled from official government records.

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Datascope Corp. recalls Battery Charging Station; Model: 0998-00-0802;

February 6, 2026 · Medical device recalls The Battery Charging Station is an optional dual-bay charger used to charge the…

Datascope Corp. recalls CS100 IABP. Software Version CS100 IABP Q.01.

January 23, 2026 · Medical device recalls Moderate risk The firm has identified that the battery runtime and cycle specifications conta…

Datascope Corp. recalls CS300 IABP. Software Version CS300 IABP C.01.

January 23, 2026 · Medical device recalls Moderate risk The firm has identified that the battery runtime and cycle specifications conta…

Datascope Corp. recalls Cardiosave Hybrid. Intra-Aortic Balloon Pump system.

November 4, 2025 · Medical device recalls Moderate risk The IFU addendum revises the Preventative Maintenance schedule to align with th…

Datascope Corp. recalls Cardiosave Rescue. Intra-Aortic Balloon Pump system.

November 4, 2025 · Medical device recalls Moderate risk The IFU addendum revises the Preventative Maintenance schedule to align with th…

Datascope Corp. recalls Cardiosave Hybrid

October 23, 2025 · Medical device recalls The IFU addendum updates the Vibration and Shock Table to reference the correct…

Datascope Corp. recalls Cardiosave Rescue

October 23, 2025 · Medical device recalls The IFU addendum updates the Vibration and Shock Table to reference the correct…

Datascope Corp. recalls MEGA 7.5Fr. 40cc Intra-Aortic Balloon with Accessories, Model Number 0684-00- 0295-01

September 17, 2024 · Medical device recalls Moderate risk There is discrepant labeling on the inner and outer packaging of the device.

Datascope Corp. recalls CARDIOSAVE HYBRID INTRA-AORTIC BALLOON PUMP (IABP). Electromechanical system used to inflate and deflate intra-aortic b…

August 8, 2024 · Medical device recalls High risk Firm has developed a software correction (Revision D.01) for outside the US to…

Datascope Corp. recalls CARDIOSAVE RESCUE INTRA-AORTIC BALLOON PUMP (IABP). Electromechanical system used to inflate and deflate intra-aortic b…

August 8, 2024 · Medical device recalls High risk Firm has developed a software correction (Revision D.01) for outside the US to…

Datascope Corp. recalls CARDIOSAVE RESCUE INTRA-AORTIC BALLOON PUMP (IABP). Electromechanical system used to inflate and deflate intra-aortic b…

August 8, 2024 · Medical device recalls High risk Firm has developed a software correction (Revision D.00) outside the US to miti…

Datascope Corp. recalls CARDIOSAVE HYBRID INTRA-AORTIC BALLOON PUMP (IABP). Electromechanical system used to inflate and deflate intra-aortic b…

August 8, 2024 · Medical device recalls High risk Firm has developed a software correction (Revision D.00) outside the US to miti…