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FDA, recall
Why did the FDA recall Cal Yee Farms' chocolates? Reasons explained
The Food and Drug Administration (FDA) issued the recall of Cal Yee Farms' chocolates on December 12, 2024. The chocolates were recalled since they may have contained undeclared ingredients.
Chocolate recall escalated to highest risk level by FDA, sold in 9 states including Ohio
FDA has elevated the recall of certain Cal Yee Farms chocolate products to a Class 1 status, the highest risk level.
FDA classifies chocolate recall to most serious level
The FDA has classified a December recall of a slew of chocolate and yogurt-covered nuts and other products as its most serious and dangerous classification.
FDA upgrades Cal Yee Farm chocolate recall to 'potential deadly'; products sold in Texas
Last month, the FDA announced a recall for multiple products from Cal Yee Farm including chocolate and yogurt covered products.
Chocolate Recall Now Classified As Potentially Deadly, According To The FDA
According to the FDA, a Class 1 recall means there is "a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
FDA sounds alarm on 'potentially deadly' Bay Area chocolate
The Food and Drug Administration has elevated three chocolates made by a Fairfield manufacturer to the highest-level recall classification.
Chocolate Recall Updated to Highest Risk Level, FDA Warns Consumption Could Cause Death
Cal Yee Farms' dark chocolate walnuts, dark chocolate almonds and dark chocolate apricots have been given a Class 1 recall classification because the chocolates contained undeclared milk
Chocolate recall elevated by FDA on products sold in Tennessee. Here's what to know
The Food and Drug Administration pushed a recall by the California-based company on multiple chocolate, yogurt and other products distributed by it due to certain allergens not being listed on the products that could cause life-threatening reactions if ingested.
FDA approves new pain medicine
FDA approves painkiller designed to eliminate the risk of addiction associated with opioids
Federal officials on Thursday approved a new type of pain pill designed to eliminate the risks of addiction and overdose associated with opioid medications like Vicodin and OxyContin. The U.S. Food and Drug Administration said it approved Vertex Pharmaceuticals’ Journavx for short-term pain that often follows surgery or injuries.
FDA Approves the First Non-Opioid Pain Drug in 20 Years
The prescription pills, sold under the brand name Journavx and made by Vertex Pharmaceuticals, are taken twice a day and represent the first new class of pain medications in 20 years—and the first non-opioid painkiller since that class first appeared on the market in the 1980s.
New non-opioid pain medication approved by FDA
( The Hill) – The U.S. Food and Drug Administration (FDA) approved Journavx (suzetrigine) oral tablets on Thursday as a first-in-class non-opioid analgesic to treat acute pain in adults.
3h
FDA recalls breadcrumbs sold nationwide over undeclared allergen
Breadcrumbs sold for months throughout the United States contain an undeclared allergen and are being recalled for safety reasons, the Food and Drug Administration announced on its website on Jan.
2d
on MSN
Pet food, raisins, and pancake mix among FDA recall list for January 2025
It's a new year, which means several new food items were deemed unsafe due to recalls by the U.S. Food and Drug ...
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on MSN
Food and Drug Administration wants to put nutrition labels front and center on food products
The U.S. Food and Drug Administration wants to put nutrition information front and center on food products to give consumers ...
JD Supra
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FDA Bans Red Dye No. 3 in Food and Ingested Drugs: What Manufacturers Should Know
On January 16, 2025, the Food and Drug Administration (FDA) issued an order banning FD&C Red No.3 in food and ingested drugs.1 Food and ingested ...
dermatologyadvisor
1d
FDA Alert: Pulmonology Drug Approvals, Recalls, and Device Updates
FDA 2025 pulmonology drug alerts, including drug approvals/warnings, vaccine approvals, and medical device recalls/updates.
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