Tag: Product safety

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.

According to Hyland's, many of their homeopathic medicines, including certain cough syrups, do not have a traditional expiration date printed on the label, a practice exempted by the FDA for homeopathic manufacturers. This means knowing "How long is Hyland's cough syrup good for?" depends on the specific product type, storage conditions, and observing for any signs of change.

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 2023, contaminated EzriCare Artificial Tears were linked to a multi-state bacterial outbreak, resulting in severe infections and vision loss. Staying informed about **which eye drops have been recalled due to contamination** is crucial for preventing harm and protecting your vision.

In 2023, a series of urgent safety alerts were issued, with the FDA reporting infections linked to contaminated eye drops that resulted in hospitalizations, vision loss, and even death. These alerts led to widespread recalls, leaving many consumers wondering what three eye drops are recalled and what actions they need to take to ensure their safety.

Over 50% of the population experiences acne at some point in their lives, leading many to seek targeted treatments like Kind Patches' hydrocolloid stickers. When considering these and other wellness products from the brand, a common question arises: are kind patches water proof? The answer is not universal and depends on the specific type of patch you are using.

In 2025, the largest eye drop recall in U.S. history affected 1.8 million products, highlighting a critical safety issue [1.2.2]. This guide answers: What eye drops for dry eyes have been recalled, and how can you protect your vision?

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.

While dietary supplements are not subject to the same stringent regulations as prescription drugs, recalls do happen for safety reasons. As of October 2025, there is no active, widespread **Emergen-C recall** in the United States, though past international recalls and legal disputes have raised consumer questions about the product's safety and marketing.

In September 2024, over 3 million tubes of Refresh P.M. and Refresh Lacri-Lube lubricant eye ointments were recalled due to a tube seal issue that could compromise sterility. Knowing which lots of Refresh PM were recalled is crucial for consumer safety, as is understanding the reasons behind these and past recalls, such as one in 2015.