Tag: Consumer alerts

According to the U.S. Food and Drug Administration (FDA), recalls are issued for products that present a risk of injury or are otherwise defective. If you're asking **What deodorant is recalled?**, you should be aware of several prominent cases, including recent voluntary recalls of Power Stick roll-on antiperspirants and a withdrawal of Mitchum roll-on deodorants in 2025.

In 2007, approximately 4 million bottles of a specific Listerine product were voluntarily recalled by its manufacturer. This widespread action was related to Listerine Agent Cool Blue Plaque-Detecting Rinse in Glacier Mint and Bubble Blast flavors.

In September 2024, a Class II recall was issued for several lots of Refresh PM lubricant eye ointment by its manufacturer, AbbVie (Allergan), addressing consumer concerns like 'Is there a recall on Refresh PM lubricant eye ointment?'. The recall was prompted by sterility concerns due to compromised tube seals, affecting over 3 million tubes across several countries.

In early 2025, a significant number of nasal spray products were subject to recalls due to potential microbial contamination and other quality issues. This has raised urgent questions for consumers, including **what nasal spray is being recalled?**, and highlights the critical importance of staying informed about medication safety alerts from the FDA and manufacturers.