News

Coffee Creamer Recalled as FDA Sets Highest Risk Level
The recalled product includes milk-derived ingredients, whey powder and casein, but does not declare milk as an allergen on ...
Over 7,000 Cases of Apple Juice Recalled Due To Possible Lead Contamination
The FDA has issued a Class II recall for Martinelli's Apple Juice due to potential mold contamination. Here's what you need ...
The FDA Issued a Class II Recall for More Than 170,000 Bottles of Apple Juice
If you've recently purchased any apple juice, then it is time to check your fridge for this important recall. The Food and ...
Coffee creamer recalled as FDA sets highest risk level across 3 states, including N.Y.
Non-dairy coffee creamer is being recalled across three states, including New York, and has been issued the highest risk ...
FDA: 63,000 Pounds of Rolled Oats Recalled Over Potential Contamination
The FDA is recalling rolled oats due to potential plastic contamination. The traditional and quick rolled oats were sold in ...
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FDA OKs Investigational New Drug Application for VS-7375 in Solid Tumors
Verastem will launch a U.S. phase 1/2a trial of oral KRAS G12D inhibitor VS-7375 after FDA IND clearance, with data to be ...
Sandwich Recall Update as FDA Sets Highest Risk Warning
Symptoms of a food allergy can include skin issues such as hives and rashes or gastrointestinal problems such as vomiting, diarrhea and stomach cramps.
Apple juice distributed in 28 states recalled over potential contamination with toxic compound: FDA
The recall has been categorized as “Class II,” meaning any contaminated product could cause “temporary or medically reversible adverse health consequences,” according to ...
Popular Men’s Multivitamin Recalled Over Undeclared Allergen, per FDA
Check your medicine cabinets: More than 7,000 bottles of Multi-V Men daily multivitamins are being recalled. The U.S. Food ...
FDA Classifies Q’Apel Medical Inc.’s Worldwide Medical Device Recall and Discontinuation of its 072 Aspiration System (Hippo) as Class I
On April 7, 2025, the U.S. Food and Drug Administration (“FDA” or “the agency”), classified Q’Apel Medical, Inc.’s (“Q’Apel” or “the company”) voluntary recall of 1,617 units of its 072 Aspiration ...