Food Giants Sued for Fueling Childhood Chronic Disease Epidemic

Lawsuit Filed Against Food Giants for Contributing to Childhood Chronic Disease Epidemic A groundbreaking lawsuit has been filed against major food companies—including Kraft Heinz, Mondelez,...

FDA Warns of Dangerous Rotarex Atherectomy Device Failures

FDA Warns of Dangerous Rotarex Atherectomy Device Failures: The U.S. Food and Drug Administration (FDA) has issued a warning regarding serious safety concerns with rotarex...

Trek Electric Bike Recall Due to Crash Hazard

Trek Electric Bike Recall Due to Crash Hazard Trek Bicycle Corporation has issued a recall for approximately 927 Electra E-bikes due to a dangerous defect...

DuraGen Dural Graft Recall; Integra LifeSciences Boston

DuraGen Dural Graft Recall; Integra LifeSciences Boston DuraGen, a dural graft matrix manufactured by Integra LifeSciences Boston, purports to protect the brain and spinal cord...

Hair Relaxer MDL Stalled

Hair Relaxer MDL Stalled as Disputes Between Parties Persisted Thousands of lawsuits have been filed against major hair relaxer manufacturers, including L’Oréal and Strength of...

Dangerous Crib Recall & What You Need to Know

Dangerous Crib Recall & What You Need to Know As parents, we all want to make sure our babies are safe, comfortable, and protected—especially when...

Permobil Wheelchair Recall – the Max Mobility Permobil SmartDrive Speed Control Dial

September 9 Update: Global expansion and full removal of all SpeedControl Dials used with the SmartDrive MX2+ Power Assist Device due to a design flaw...

Philips Cardiac Telemetry Recall: Updated FDA Classification

Philips Cardiac Telemetry Recall: Updated FDA Classification and What It Means for Patients The FDA escalated its recall classification for Philips’ outpatient cardiac telemetry system...

Important Recall for John Deere ZTrak Zero Turn Mowers

Important Recall for John Deere ZTrak Zero Turn with Kawasaki Engines John Deere has issued a recall for approximately 39,000 ZTrak Zero Turn mowers equipped...

BioZorb Recall – FDA’s Warning Letter to Hologic, Inc.

BioZorb Recall - FDA Warning Letter to Hologic, Inc.: What It Reveals About the BioZorb Marker Update concerning the BioZorb recall. On December 18, 2024,...

Consumer Alerts

Food Giants Sued for Fueling Childhood Chronic Disease Epidemic

FDA Warns of Dangerous Rotarex Atherectomy Device Failures

Trek Electric Bike Recall Due to Crash Hazard

DuraGen Dural Graft Recall; Integra LifeSciences Boston

Hair Relaxer MDL Stalled

Dangerous Crib Recall & What You Need to Know

Permobil Wheelchair Recall – the Max Mobility Permobil SmartDrive Speed Control Dial

Philips Cardiac Telemetry Recall: Updated FDA Classification

Important Recall for John Deere ZTrak Zero Turn Mowers

BioZorb Recall – FDA’s Warning Letter to Hologic, Inc.

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