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Maquet Cardiovascular Us Sales, Llc: Medical Device Recalls in 2018

Updated on March 25, 2026.

According to to data from the FDA, there were 2 medical device recalls made by Maquet Cardiovascular Us Sales, Llc in 2018. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.
See this for other years:
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2018
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  • QUADROX-i Neonatal without integrated arterial filter and VHK 11000 (VKMO 10000-USA#QUADROX-i Neo.+Reservoir), Part Number 701055120 The membrane oxygenator QUADROXi Neonatal is intended for use in extracorporeal circulation during cardiopulmonary bypass in cardiac surgery.
  • QUADROX-i Neonatal with integrated arterial filter and VHK 11000 (VKMO 11000-USA#QUADROX-i Neo.+Reservoir), Part Number 701055207 The membrane oxygenator QUADROXi Neonatal is intended for use in extracorporeal circulation during cardiopulmonary bypass in cardiac surgery.
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