Brand Recall Hub

Cardiosave Recalls in Canada

12 recalls found for Cardiosave. Data sourced from Health Canada, CFIA, and Transport Canada. Updated daily.

12 Cardiosave Recalls

Medical Devices Type II
2023-08-18

Datascope Cardiosave Hybrid And Rescue Intra-Aortic Balloon Pumps (IABP)

Performance

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Medical Devices Type I
2023-08-14

Cardiosave System - Hybrid & Rescue Intra-Aortic Balloon Pump

Performance

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Medical Devices Type II
2023-06-16

Datascope Cardiosave Hybrid And Rescue Intra-Aortic Balloon Pumps (IABP)

Performance

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Medical Devices Type II
2023-03-16

Cardiosave System - Hybrid & Rescue Intra-Aortic Balloon Pump

Performance

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Medical Devices Type II
2023-02-17

Cardiosave System - Hybrid & Rescue Intra-Aortic Balloon Pump

Performance

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Medical Devices Type II
2023-01-04

Cardiosave System - Hybrid & Rescue Intra-Aortic Balloon Pump

Performance

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Medical Devices Type II
2021-12-13

Cardiosave System - Hybrid & Rescue Intra-Aortic Balloon Pump

Manufacturing defect

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Medical Devices Type II
2021-10-01

Cardiosave System - Battery Only (2021-09-23)

Medical devices

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Medical Devices Type II
2021-09-24

CARDIOSAVE SYSTEM - HYBRID & RESCUE INTRA-AORTIC BALLOON PUMP (2021-09-14)

Medical devices

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Medical Devices Type I
2019-07-09

CS300, CS100, Cardiosave Hybrid, and Cardiosave Rescue IABP (2019-07-02)

Medical devices

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Medical Devices Type II
2018-11-02

Cardiosave Hybrid IABP (2018-09-26)

Medical devices

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Medical Devices Type II
2018-05-25

CARDIOSAVE Intra-Aortic Balloon Pump (IABP) (2018-05-08)

Medical devices

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