Tag: Drug recall

Starting in 2020, the U.S. Food and Drug Administration (FDA) initiated recalls for certain batches of extended-release (ER) metformin due to the presence of N-nitrosodimethylamine (NDMA) above acceptable limits. This action led to confusion about why is metformin being taken off the market, but it was a targeted safety measure by manufacturers, not a market-wide ban.

In March 2000, the first thiazolidinedione (TZD) approved for type 2 diabetes was voluntarily withdrawn from the market after being linked to at least 63 liver-failure deaths, causing many to ask: Which TZD was discontinued and why?.

According to a resource compiling drug withdrawal data, more than 578 drugs have been withdrawn or discontinued from markets globally due to various reasons, with safety issues being a primary cause. This highlights the critical nature of understanding what medications have been discontinued and why.

In 2022, a major nationwide recall was issued for liquid magnesium citrate oral solutions due to contamination with the bacterium *Gluconacetobacter liquefaciens*, leading to its widespread unavailability. This article explores the specifics of the recall, its implications, and explains why is magnesium citrate no longer available at many major retailers.

Between 1953 and 2013, 462 medications were withdrawn worldwide, primarily due to adverse reactions [1.9.4]. Understanding what drugs are discontinued involves looking at safety, efficacy, and commercial factors that lead to their removal from the market.

Over the last century, a significant number of drugs have been voluntarily withdrawn by manufacturers or mandated by regulatory agencies, primarily due to adverse drug reactions and other safety issues. Understanding why a medication is no longer available is crucial for patient safety, as many factors beyond a safety recall can influence which medications are discontinued.

From 2013 to 2018, nearly 8,000 medications were recalled by pharmaceutical companies [1.8.5]. Several of these have been prominent painkillers. So, what pain medication was removed from the market, and for what reasons? This reveals much about post-market drug safety.

While no widespread, active recall for all fluticasone propionate nasal sprays is currently in effect, several manufacturers have initiated recalls for specific batches and products in recent years. These have ranged from manufacturing errors like glass particles to quality control issues and company shutdowns.

The U.S. Food and Drug Administration (FDA) recommends that consumers do not use any products containing phenylpropanolamine due to its association with an increased risk of hemorrhagic stroke. Therefore, the question of **how many days should I take phenylpropanolamine?** is moot, as it is no longer available for human use in the U.S..

Recent eye drop recalls have underscored the severe dangers of contaminated products; in 2023, the CDC and FDA linked certain brands to infections, vision loss, and even death. Understanding what happens if you use bad eye drops is critical for protecting your ocular health.