Brand Recall Hub

Intra Aortic Recalls in Canada

15 recalls found for Intra Aortic. Data sourced from Health Canada, CFIA, and Transport Canada. Updated daily.

15 Intra Aortic Recalls

Medical Devices Type I
2024-05-07

Ultra Intra-Aortic Balloon Pumps (IABP)

Performance

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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
2021-09-24

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

Medical devices

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Medical Devices Type II
2020-09-11

INTRA-AORTIC BALLOON CATHETERS (2020-08-28)

Medical devices

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Medical Devices Type II
2020-06-12

Arrow AutoCAT 2 & AC3 Optimus Intra-Aortic Balloon Pump (2020-05-22)

Medical devices

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Medical Devices Type I
2019-07-16

IntraClude Intra-aortic Occlusion Device (2019-05-22)

Medical devices

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Medical Devices Type II
2019-03-08

IntraClude Intra-Aortic Occlusion Device (2019-01-21)

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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Medical Devices Type II
2018-05-18

IntraClude Intra-aortic Occlusion Device (2018-04-02)

Medical devices

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