The Financial Express1 小时
FDA Alert: Millions of granola bars recalled over metal contamination; Classified as class ...
Certain batches of MadeGood granola bars were recalled due to the potential presence of a piece of metal in the product, ...
MLive9 小时
FDA raises risk level on recall of 2 million cases of granola bars sold nationwide
The Food and Drug Administration last week elevated the risk level for more than two million cases of recalled granola bars ...
KELOLAND News12 小时
‘May contain metal pieces’: FDA updates recall for granola bars sold nationwide
The U.S. Food and Drug Administration has posted an update on a granola bar recall initiated last year, labeling it as “Class ...
The Mirror US on MSN12 小时
Pancake mix recall skyrockets to highest risk level after FDA warns of milk allergen
The original recall has since been upgraded to Class I, which denotes the highest risk level in connection to a pulled ...
A pancake mix is being recalled by the FDA. Does it affect Ohio retailers? What to know
A pancake mix by Quaker Oats is being recalled for a deadly undeclared allergen. Is Ohio affected? Here's how to check.
Pancake mix recall hits highest danger level: Does it affect Pa.?
According to Forbes, Pearl Milling Company — which is part of the Quaker Oats family — voluntarily pulled 10,000 cartons of ...
FDA recalls millions of granola bars for a ‘potential presence of metal’
A food distributor is recalling certain batches of granola bars due to potential contamination involving a metal object, ...
FDA sets highest risk level for recall on popular pancake and waffle mix
The U.S. Food and Drug Administration classified the Pearl Milling Company Original Pancake & Waffle Mix recall as a Class I.
Waffle Recall Update as FDA Sets Highest Risk Level
Eating the recalled waffles could cause "serious adverse health consequences or death" for some consumers, according to the FDA.
devdiscourse20 小时
Major Recalls: Glenmark and FDC Tackle USFDA Warnings
Glenmark Pharmaceuticals and FDC Ltd are withdrawing products in the US due to manufacturing problems, as per USFDA reports.