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Maquet Cardiopulmonary Ag Recalls
5 recalls on record · May 16, 2018 to June 4, 2025 · Medical Devices
Recalls by year
18
25
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
June 4, 2025Medical DevicesFDA
Maquet Cardiopulmonary Ag recalls Cardiohelp System HKH 8820 Wall Holder. Mounting bracket designed to hold the CARDIOHELP-i system for interhospital tran
Hazard: HKH 8820 Wall Holder does not comply with standard DIN EN 1789:20 and has the potential to detach.
June 20, 2018Medical DevicesFDA
Maquet Cardiopulmonary Ag recalls Aortic Arterial Cannula 24 Fr (O.D.); 23 cm (L); with 3/8-inch connector with LL, Part Number 701002267, Article Number
Hazard: This lot of arterial cannula may have been supplied with 3/8-width de-airing plugs that could break during the process of removal from the arterial cannula.
June 20, 2018Medical DevicesFDA
Maquet Cardiopulmonary Ag recalls Aortic Arterial Cannula 22 Fr (O.D.); 23 cm (L); with 3/8-inch connector with LL, Part Number 701002246, Article Number
Hazard: This lot of arterial cannula may have been supplied with 3/8-width de-airing plugs that could break during the process of removal from the arterial cannula.
June 20, 2018Medical DevicesFDA
Maquet Cardiopulmonary Ag recalls Aortic Arterial Cannula 20 Fr (O.D.); 23 cm (L); with 3/8-inch wide connector, Part Number 701002206, Article Number A20
Hazard: This lot of arterial cannula may have been supplied with 3/8-width de-airing plugs that could break during the process of removal from the arterial cannula.
May 16, 2018Medical DevicesFDA
Maquet Cardiopulmonary Ag recalls CARDIOHELP Gas Bottle Holder HKH 8880, Product Code/Part Number 70105.0901 Product Usage: The Cardiohelp Gas Bottle
Hazard: There is a possibility for the clamps of the gas bottle holder to crack or break when exposed to strong vibrations.