Tag: Recall

In 2020, the U.S. Food and Drug Administration (FDA) issued voluntary recalls for several lots of extended-release (ER) metformin due to contamination, not a nationwide ban. The action targeted specific batches from certain manufacturers that contained unacceptable levels of the impurity N-Nitrosodimethylamine (NDMA), a probable human carcinogen, but left other metformin products on the market.

In 2021, manufacturer Pfizer voluntarily recalled all lots of the brand-name medication Chantix (varenicline), leaving many to question, “Do they still prescribe Chantix for smoking?”. While the brand-name product was permanently discontinued, generic versions of varenicline are still widely prescribed and considered safe and effective by regulatory bodies.

Following a series of recalls by the U.S. Food and Drug Administration (FDA) that began in 2018, many patients have been left wondering, "Is losartan being taken off the market?". The simple answer is no; while specific lots were recalled due to potential impurities, the medication as a whole remains widely available and is still prescribed for treating high blood pressure.

Since 2023, the FDA has coordinated several eye drop recalls impacting numerous brands due to serious contamination and manufacturing issues. This article provides a crucial breakdown of **what brands of eye drops are recalled** and why, to help protect your eye health.

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.

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.

As of October 2025, a recall for the prescription medication Xiidra has not been issued. However, confusion may stem from a specific recall of *over-the-counter* (OTC) eye drops and past manufacturing issues, leading many to ask, 'Has Xiidra been recalled?'.

In July 2022, a major nationwide recall removed liquid magnesium citrate laxatives from store shelves due to bacterial contamination from manufacturer Vi-Jon. This significant event explains **why is magnesium citrate so hard to find** in its oral solution form at major retailers and pharmacies like CVS and Walgreens.

Following a widespread recall in 2020, the manufacturer of Nature-Throid discontinued the product in 2024, meaning it is no longer available for prescription. This has left many patients searching for answers and alternative treatment options for their hypothyroidism.

In early 2023, the Centers for Disease Control and Prevention (CDC) linked an outbreak of a rare, drug-resistant bacteria to two types of artificial tears, leading to severe health outcomes, including blindness. For those asking which two eye drops are recalled in this major event, the products were EzriCare Artificial Tears and Delsam Pharma Artificial Tears. While this specific incident involved two key products, numerous other eye drop recalls have been issued by the FDA in recent years due to various contamination and manufacturing issues, underscoring the importance of staying informed about product safety.