Face Moisturizer Recalled Nationwide as FDA Sets Risk Level
On December 23, First Aid Beauty recalled 2,756 jars of its Ultra Repair Cream. According to the FDA, a deviation from ...
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Nationwide Recall Issued For Popular Corn Puff Product
A nationwide recall has been issued for a popular snack brand. Wismettac Asian Foods, Inc. has issued a nationwide recall of ...
Milk Recall Update As FDA Sets Risk Class Over Spoilage Fears
The recall was voluntarily initiated by the firm on December 13 last year and on January 17, the milk products were issued a ...
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FDA Warns Clinicians Not to Confuse Epinephrine Products Due to Similar Packaging
Similarities between the packaging for certain intranasal and intravenous epinephrine products may result in inappropriate administration.
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FDA issues highest risk level recall for over 6,000 tubs of protein powder
Orgain has issued a Class I recall for its 30g Plant Protein Complete Protein Powder due to undeclared peanut allergens. The ...
Yogurt Recall Update As FDA Sets Risk Level Over Plastic Contamination
Greek yogurt has been recalled because it may contain foreign objects, given the FDA's second-most severe risk level.
FDA finds little handwashing, dirty equipment at McDonald's supplier linked to E. coli outbreak
More than a hundred E. coli cases were linked to contaminated onions produced by Taylor Farms used in McDonald's burgers.
Pancake, waffle mix recall: What consumers need to know
Those with an allergy or severe sensitivity to milk run the risk of severe allergic reaction, according to the FDA.
FDA recalls pancake mix in Kansas and 10 other states. Here's why.
The FDA recalled Pearl Milling pancake and waffle mix earlier this week. Products were on the shelves as early as Nov. 18, ...
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FDA recalls popular eye drops for fungal contamination
Fort Worth, Texas-based Alcon Laboratories has voluntarily recalled one lot of Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, which are packaged in batches of 25.
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FDA warns Hologic to do more to prevent harm from component in recalled implant markers
The U.S. Food and Drug Administration has sent a warning letter to Marlborough, Mass.-based medical technology company ...
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Philips has a serious cardiac monitoring software recall
The FDA announced today that a Philips recall involving remote cardiac monitoring software is Class I, its most serious ...