Tag: Fda recall

Affecting millions with hypothyroidism, the stability of levothyroxine is critical for patient health. A primary reason for recent instances where patients asked, 'Why was there a recall on levothyroxine?' relates to the medication's sensitive nature, which can cause its active ingredient to degrade over time, a problem known as subpotency.

In recent years, several birth control pills have been voluntarily recalled for issues ranging from packaging errors to reduced effectiveness [1.2.1, 1.2.3, 1.2.5]. Knowing which birth control pills have been recalled is crucial for ensuring contraceptive efficacy and personal health.

In recent years, the U.S. Food and Drug Administration (FDA) has overseen the recall of dozens of over-the-counter eye drop products, raising consumer concerns [1.5.1]. This environment of heightened scrutiny leads many to ask: **Has Refresh eye drops been recalled?**

Following a 2000 public health advisory by the FDA, consumer products containing phenylpropanolamine (PPA) were voluntarily withdrawn from the market in the United States due to an increased risk of hemorrhagic stroke. This advisory and subsequent removal mean that no one should take phenylpropanolamine for human use, especially those with preexisting cardiovascular conditions.

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.

In 2000, the U.S. Food and Drug Administration (FDA) issued a public health advisory recommending against human use of phenylpropanolamine (PPA) due to its association with an increased risk of hemorrhagic stroke. This action effectively ended its widespread use in over-the-counter cold medicines and appetite suppressants, but it begs the question: what can phenylpropanolamine be used for today? The answer lies predominantly in veterinary medicine, where the drug continues to be an approved treatment for certain conditions in animals.

In April 2020, the FDA requested the removal of all ranitidine products, including the original Zantac, from the market due to safety concerns. The crucial distinction is that **Pepcid the same as Zantac** question can be answered by understanding their different active ingredients, with Pepcid containing famotidine and the original Zantac containing ranitidine.

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.

While there have been recalls of artificial tears in recent years, affecting numerous brands due to contamination concerns, an important distinction must be made regarding the history of GenTeal gel. The answer to "Has GenTeal gel been recalled?" is yes, but the specific recalls involving GenTeal occurred nearly two decades ago and are separate from the more recent and widely publicized industry-wide alerts.