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All product recalls associated with Maquet Medical Systems USA.
Total Recalls
1000
Past Year
1000
Class I (Serious)
34
Most Recent
Jan 2026
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
The Bubble Sensor optional accessory to the CARDIOHELP-i extracorporeal life support system includes an incorrect UDI Device Identifier (DI) provided with the label attached to the device.
Mobile x-ray systems moving arm frame welding issue which presents the potential of bodily harm due to fall of the arm.
This recall involves BlendJet 2 Portable Blenders sold in a variety of colors and designs. Serial numbers are printed on the bottom of the base along with "blendjet2" and "The Original Portable Blender." The blenders measure approximately 9.5 inches in height and 3 inches in width and weigh approximately 1.5 pounds. Units where the first 4 digits of the serial number are between 5201-5542 and are subject to the recall must be identified through the use of the "Is my BlendJet 2 Recalled?" tool located at www.blendjet.com/safetyandrecall.