Maquet Medical Systems USA: Medical Device Recalls in 2024

Updated on March 25, 2026.

According to to data from the FDA, there were 6 medical device recalls made by Maquet Medical Systems USA in 2024. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

Bubble Sensor (REF: 70105.5720)
BEQ-RF-32-USA RotaFlow Centrifugal Pump with BIOLINE Coating, Product Code 701047554. For use with an extracorporeal cardiovascular or cardiopulmonary bypass circuit.
BO-RF-32-USA RotaFlow Centrifugal Pump with SOFTLINE Coating, Product Code 701047553. For use with an extracorporeal cardiovascular or cardiopulmonary bypass circuit.
Model No. BEQ-HLS 5050 USA, HLS Set Advanced 5.0, Product Code/Part Number 70106.9077. Used with the CARDIOHELP heart-lung machine.
CARDIOHELP-i System. Blood oxygenation and carbon dioxide removal system.
BEQ-HLS 7050 USA, HLS Set Advanced 7.0, Product Code/Part Number 70106.9078. Used with the CARDIOHELP heart-lung machine.