Food Recalls, Updates March 14: H-E-B Dip, Chocolate Nut's Risk Level Set
A recalled spinach artichoke dip is a Class II risk, and updates have been issued for the recall of chocolate nut and wafer ...
The U.S. Food and Drug Administration increases risk level to recalled coffee creamers
The Food and Drug Administration has increased the risk level of two coffee creamers recalled in late February. Approximately ...
Canned tuna recall: FDA updates risk level for products sold at major retailers, including Costco, Walmart
The U.S. Food and Drug Administration (FDA) posted a notice in February that Tri-Union Seafoods is recalling select lots of ...
Health on MSN9h
Recalls You May Have Missed This Week: Coffee Creamer, Sparkling Water, and More
This week saw four large-scale recalls over a range of issues, from chemical concerns to foreign material contamination.
More Than 75K Bottles of International Delight Coffee Creamer Recalled Due to ‘Complaints of Spoilage and Illness’
The recalled International Delight products were distributed to 31 states across the U.S., including Florida, Georgia, New ...
La Roche-Posay, Walgreens, Proactiv and More Voluntarily Recall Acne Treatments Due to Trace Amounts of Cancer-causing Benzene
La Roche-Posay, Walgreens, Proactiv and SLMD Skincare have voluntarily recalled acne treatments from retail that contained ...
Scientific American3d
Are Foodborne Illnesses and Deaths in the U.S. Worsening? New Data on Recalls Explain
Despite headlines, there were fewer food recalls in 2024 than in 2023, but more people died from food poisoning linked to ...
Recall alert: Popular coffee creamer recalled — throw away now
Two flavors of a popular coffee creamer brand have been recalled due to spoilage and illness concerns, according to the FDA.
Drinking Water Recall Update as Courts Get Involved
Numerous lawsuits have been filed against the company in the years since it was recalled, alleging that the company's ...
The BMJ2d
Late adverse event reporting from medical device manufacturers to the US Food and Drug Administration: cross sectional study
Objective To describe the extent of late adverse event reporting by manufacturers to the US Food and Drug Administration’s (FDA) Manufacturer And User Facility Device Experience (MAUDE) database as ...