The FDA recall notice has been categorized as Class 1, the highest risk level that can lead to adverse health affects and ...

The recall has been given a Class II classification, indicating there is a significant level of risk posed to consumers in ...

The status of the recall is ongoing. According to the FDA, "A recall is an action taken by a company to correct or remove from the market an FDA regulated product that violates U.S. laws and ...

On Thursday, July 10, the U.S. Food and Drug Administration announced a nationwide recall of some Power Stick deodorants, manufactured by A.P. Deauville. The recall was voluntary and involves 21,265 ...

Dublin, July 24, 2025 (GLOBE NEWSWIRE) -- The "FDA Recalls - Before You Start, and After You Finish" training has been added to ResearchAndMarkets.com's offering.Understanding FDA's Recall ...

There are 168,632 tubes and 13,092 kits affected, according to the FDA’s recall database. The devices are used to help patients breathe by draining fluids from the upper part of the windpipe.

They add that "recalls may be initiated voluntarily by a company, or at the request of the FDA." More than 83,000 FDA regulated products were recalled between the years 2014 and 2024.

FDA recalls over 67,000 cases of Power Stick deodorant. See where products were sold By Marley Malenfant, Austin American-Statesman Updated July 18, 2025 8:44 a.m.