FDA Finds Drug Missing Main Ingredient in Random Testing
The Food and Drug Administration has banned the use of a particular batch of the drug Frusemide, used as a diuretic, after finding a batch was missing the main ingredient during random testing, according to news sources. The drug, which is used in patients with liver, kidney, and heart problems, was found to have defects… read more
Source of Listeria Contaminiation Confirmed
The U.S. Food and Drug Administration has confirmed that they found the source of a multiple state outbreak of listerosis in samples of Jensen Farms’ Rocky Ford-brand cantaloupe, according to news reports. Tests were taken at a Denver store and at Jensen’s packing warehouse. The samples matched one of three strains that have been found… read more
FDA Announces Safety Review, Re-labeling of Ondansetron Drug
The Food and Drug Administration has announced a safety review of the drug ondansetron, an anti-nausea medication, often prescribed to patients of chemotherapy, radiation therapy, and those who have undergone recent surgery. Studies indicate that ondansetron can increase the chances of prolongation of the QT interval of the electrocardiogram, which can lead to irregular heart… read more
E. coli Contamination Spurs Raw Milk Recall
Pride & Joy Creamery has issued a recall for raw fluid milk due to a potential E. Coli contamination, according to news sources. The milk affected was sold in nine different Puget Sound stores in King, Pierce, Snohomish, and Skagit counties and include Sno-isle in Everett, Truhealth in Bothell, Marlene’s Market in Tacoma and Federal… read more
Bus Accident Victim Settles for $10.5 Million
Los Angeles Personal Injury Lawyer Brian Panish of Panish | Shea | Ravipudi LLP reached a record $10.5 million settlement with AC Transit shortly before the lawsuit was set for trial. Three years after its occurrence, a bus accident that severely injured a pedestrian will cost AC Transit $10.5 million dollars, according to news sources…. read more
Marine Corps Contractors Cited for Safety Hazards
Chevron Energy Solutions, Inc., Piedmont Mechanical Inc., and Jim Boyd Construction Inc. have all been cited by the Occupational Health and Safety Administration after a worker received burns at a U.S. Marine Corps Base in Georgia, according to news reports. An inspection found the companies to be in violation of three willful and eight serious… read more
FDA Halts Production of Supplements Making Unapproved Claims
The FDA has stopped a company from distributing amino acid products that they marketed as treatment for neurotransmitter diseases such as Parkinson’s And Alzheimer’s, according to news sources. West Duluth Distribution subsidiaries CHK Nutrition and NeuroResearch Clinics were found to be selling products making unapproved claims in July 2010. Besides Parkinson’s and Alzheimer’s the products… read more
Sprint Offers App to Disable Phone While Driving
Sprint is offering an app for their Android phones that they hope will prevent distracted driving that stems from cell phone use, according to news sources. The app, called Drive First, will be available to Blackberry phone soon, and currently costs $2 a month. Sprint is targeting the app toward teen parents, who can download… read more
Truckers to be Banned from Cell Phone Use?
According to recent news reports, the National Transportation Safety Board has recommended that commercial truck drivers be banned from using cell phones while driving, including hands-free devices. The recommendation comes after news that a Kentucky driver whose fatal crash killed ten other people was making calls on his cell phone during the accident. Reports indicate… read more
Subaru Recalls 2011 Vehicles Due to Defective Sunroof
Subaru has announced a recall of their 2011 Outback and Legacy vehicles due to a defective sunroof issue that increases the risk of a crash, according to news sources. Approximately 69,590 Outback and Legacy vehicles are involved in the recall. The cars were manufactured from August 3, 2010 to July 1, 2011. The sunroofs on… read more
Transvaginal Mesh Review May Revoke FDA Approval
The U.S. Food and Drug Administration has issued a report announcing their recommendation that transvaginal mesh devices be re-classified as a high risk medical device, according to news sources. The FDA is requiring new safety statistics be submitted by the manufacturer in order for the product to remain on the market. A panel will meet… read more
Study Shows Many Patients Believe FDA Approves Only Safe Drugs
A recent study examines patients and their belief that the U.S. Food and Drug Administration only approves safe and effective drugs. The study found that providing more information to consumers can help them make better choices, according to a news article. Two doctors investigated how U.S. consumers make drugs choices through an Internet-based trial of… read more
