News

Pickles Recall Update As FDA Issues Risk Warning
The recall has been given a Class II classification, indicating there is a significant level of risk posed to consumers in ...
Nationwide Ritz cracker recall update as FDA issues risk warning
Mondelēz Global announced a recall for various sizes of Ritz peanut butter cracker sandwiches over possible undeclared ...
FDA Upgrades Recall on 160,000+ Bottles of Thyroid Medication
The recall of more than 160,000 bottles of levothyroxine sodium, which went into effect June 20, was upgraded to a Class II ...
FDA Recalls Single-Serve Coffee Pods Over Potentially Toxic Brewing Risk
FDA Recalls Single-Serve Coffee Pods Over Potentially Toxic Brewing Risk originally appeared on Men's Fitness. Keurig users, ...
Sun Pharma, Lupin, Dr Reddy's recall products in US market due to manufacturing issues
Three major Indian pharmaceutical companies are recalling drugs in the United States. Sun Pharma is recalling ...
FDA Announces Major Recall of Popular Deodorant
It's important to stay informed about recalls, because doing so truly impacts your life. Of course, the sooner you know about ...
FDA deodorant recall issued for thousands of cases sold nationwide: What to know
Three roll-on deodorant products were recalled earlier this month due to deviations from regulations on manufacturing set by ...
FDA announces recall of more than 110,000 ice cream bars sold in 23 states, including Pennsylvania
WASHINGTON D.C., DC — A Florida ice cream company has voluntarily recalled more than 110,000 ice cream bars and frozen ...
FDA Recalls More Than 67,000 Cases of Deodorant
Various Power Stick deodorants have been recalled due to "Current Good Manufacturing Practice deviations", according to the U ...
FDA recalls over 67,000 cases of Power Stick deodorant. See where products were sold
The manufacturer announced a recall of 67,214 cases of its Power Stick roll-on deodorant due to violations of Current Good ...
FDA Issues Risk Warning for Bread Recall Update
The FDA's assessment of the bread recall has designated it as a Class II risk, which means the product "may cause temporary ...
Sun Pharma, Lupin, Dr Reddy's recall products in US market
Sun Pharma recalls Dimesylate capsules, Lupin recalls Lisinopril and Hydrochlorothiazide tablets, and Dr Reddy’s recall Omeprazole Delayed-release capsules.