FDA Report Shows Jeni’s Splendid Ice Creams Failed To Adequately Comply With Testing, Cleaning Procedures

FDA Report Shows Jeni’s Splendid Ice Creams Failed To Adequately Comply With Testing, Cleaning Procedures

While Jeni’s Splendid Ice Creams prepares to reopen its scoop shops this weekend, newly released federal investigation reports show the Ohio-based company’s issues date back several years before its public battle with listeria contamination. [More]

(Teresa RS)

New FDA Rule Would Provide More Information About Antibiotics In Farm Animals, But Still Not Enough

After decades of inaction on the issue, the FDA is slowly taking actions that it hopes will curb the overuse of antibiotics in farm animals, which currently accounts for around 80% of all antibiotics sold in the U.S. The agency’s latest measure, if approved, will provide more information about how farmers are using these medically important drugs, but by the FDA’s own admission, it’s still not sufficient. [More]

FDA Finally Warns Drug Company Against Selling Antibiotic As A Pig-Fattener

FDA Finally Warns Drug Company Against Selling Antibiotic As A Pig-Fattener

A year after public health advocates called out drug maker Novartis for continuing to actively market a particular antibiotic as a product farmers could use to fatten up their pigs, the FDA has finally gotten around to issuing a warning. [More]

(Scoboco)

Johnson & Johnson Creating An Independent Panel To Review Patient Requests For Unapproved Drugs

What’s a sick person to do when all the drugs on the market haven’t been able to help ease their ailment? Some of the seriously ill turn to medical trials held by drug companies to gain access to experimental drugs, but it’s not always easy to accomplish. A new system from Johnson & Johnson will employ an independent panel to review requests from seriously ill people who want to try an unapproved drug without participating in the actual testing of the drug. [More]

These are four of the 16 supplements the FDA has targeted in its latest crackdown of dietary supplements with potentially dangerous ingredients.

FDA Continues Crackdown On Dietary Supplement Ingredients, Notifies Makers Of 16 Products To Stop Sales

A week after the Food & Drug Administration heeded calls for action by scientists and health advocates by demanding that dietary supplement makers stop selling products with a speed-like ingredient, the agency sent another warning to 14 manufacturers asking them to cease the sale of several products with another possibly harmful stimulant. [More]

FDA Warns Makers Of Diet Supplements Containing Speed-Like Ingredient

These are four of the eight products cited in the FDA warning letters.

Following calls for action from scientists and consumer health advocates, the FDA has sent warning letters to a handful of diet supplement makers demanding that they cease selling products that contain a speed-like ingredient. [More]

Tobacco Companies Sue FDA Over Cigarette Packaging Guidelines

(mendhak)

For more than 5 years, the FDA has had authority to regulate tobacco products, and last month, the agency issued guidance to the tobacco industry about when cigarette makers must seek FDA approval on changes to packaging. The country’s largest tobacco businesses now believe the FDA is overstepping its authority and violates their rights to free expression. [More]

(Mike Mozart)

FDA To Health Food Companies: The Word ‘Healthy’ Has An Actual Meaning

Kind bars are quite tasty, but are they healthy? Sure, they’re made from ostensibly healthy ingredients like nuts and dried fruit, but some bars also have ingredients like chocolate and peanut butter. The Food and Drug Administration sent the company a warning letter about their use of the word “healthy” to describe their snacks on the label. [More]

Makers Of SmartCandy Warned About Possibly Misleading Nutrition Claims

Makers Of SmartCandy Warned About Possibly Misleading Nutrition Claims

The Attorney General’s office for the state of New York is cautioning the company behind “vitamin infused snack” SmartCandy that its advertising may run afoul of state and federal regulations, according to a letter obtained by Consumerist. [More]

FDA: Antibiotic Use In Farm Animals Grew In Spite Of Regulation

FDA: Antibiotic Use In Farm Animals Grew In Spite Of Regulation

Back in 2012, the FDA banned “extra-label” non-medical use in animals for the cephalosporin class of antibiotics, which are commonly used to treat humans for pneumonia, urinary tract infections, and other maladies. Not only did this restriction fail to curb the use of cephalosporins, but a new FDA report shows that the drug use increased following the ban. [More]

Sabra Recalling 30,000 Cases Of Classic Hummus Over Listeria Fears

Sabra Recalling 30,000 Cases Of Classic Hummus Over Listeria Fears

Whether you like to dip pita chips or veggies, pretzels or just your fingers, check that hummus package before you go snacking: Sabra is recalling 30,000 cases of its classic flavor of hummus sold nationwide over fears that the product could be tainted with listeria. [More]

Blue Bell Expands Recall Again After Tests Find Listeria Bacteria In Additional Products

Blue Bell Expands Recall Again After Tests Find Listeria Bacteria In Additional Products

It appears that grocers who removed all Blue Bell Creameries’ products from their shelves earlier this week may have had the right idea, as the ice cream company once again expanded the scope of its recall after further testing found a link between additional products and an outbreak of listeriosis. [More]

(kreezzalee)

White House Acknowledges Health Risk Of Antibiotics Overuse; Critics Say It Fails To Fully Address Problem

In a new White House report on antibiotic resistance, the Obama administration acknowledges the serious public health risk posed by the over-prescription and overuse of antibiotics, and details multi-agency plans to combat the problem. However, many critics of the report say that these plans fail to close a loophole that will allow farmers to continue using medically unnecessary antibiotics on farm animals (who consume 80% of all antibiotics sold in the U.S.) primarily for the purpose of growth promotion. [More]

Blue Bell has recalled a number of products that may be linked to listeria infections in Kansas.

Health Officials Link Blue Bell Ice Cream Products To Listeriosis Outbreak; Company Recalls Treats

Three months after candy apples contaminated with Listeria bacteria were linked to seven deaths, another sweet treat may contain the bacteria and could be a contributing factor in at least three deaths. [More]

FDA Warns That Chantix May Decrease Users’ Alcohol Tolerance

FDA Warns That Chantix May Decrease Users’ Alcohol Tolerance

Smokers using the prescription drug Chantix (varenicline) to help them through the quitting process may want to sip their beers slowly, as this week the FDA approved new warnings that the drug can change the way users react to alcohol. [More]

(Carbon Arc)

Father Of Teen Poisoned By Caffeine Powder Files Lawsuit Blaming His Death On Supplement Makers, Amazon

The father of an Ohio teen who died in 2014 after ingesting a powdered caffeine marketed as a dietary supplement has filed a lawsuit against Amazon.com and the product’s distributors, claiming that they failed to provide proper warnings about the dangers of using the substance. [More]

(D O'Quinn)

FDA Approves First “Biosimilar” Drug. Could Drive Down Cost Of Most Expensive Medications

Biotech drugs — which are generally derived from a living organism, as opposed to traditional purely chemical medications — are currently among the most expensive medicines available. But today, the Food and Drug Administration issued its first approval of a drug that is “biosimilar” to an existing biotech medication; a development that could possibly result in billions of dollars in savings. [More]

FDA Warns: If Your “Low T” Is Just From Getting Older, Don’t Use Prescription Testosterone

FDA Warns: If Your “Low T” Is Just From Getting Older, Don’t Use Prescription Testosterone

In recent years, makers of prescription testosterone treatments like AndroGel began throwing around the term “Low T” in TV ads, blaming low levels of the hormone for various problems — sex drive, flagging energy, moodiness — that have long been associated with simply growing older. But the FDA is now acknowledging that these drugs pose “a possible increased risk of heart attack and stroke” and are warning against their use for the treatment of anything other than very specific medical conditions. [More]