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Quick answer: In September 2026, Centric Compounding of Houston, Texas recalled six lots of injectable vials: three of Glutathione 200 mg/mL, two…
Continue reading »Quick answer: On August 19, 2026, Optimal Balance Pharmacy of Houston, Texas recalled one lot of compounded glutathione injection, lot LG342009076, after…
Continue reading »Quick answer: On August 5, 2026, Victory Medical Center Pharmacy of Austin, Texas recalled three lots of compounded glutathione 200 mg/mL after…
Continue reading »Quick answer: On August 27, 2026, the FDA told compounding pharmacies not to use dietary supplement grade glutathione to make injectable drugs.…
Continue reading »Quick answer: On October 1, 2026, Greenwich Rx, a compounding pharmacy in Tomball, Texas, recalled ten lots of Glutathione Injection 200 mg/mL…
Continue reading »Mylan today issued a statement announcing that it is taking immediate action to increase access to EpiPen® Auto-Injectors by expanding already existing programs in recognition of those patients who are facing the burden of higher out-of-pocket costs, reducing direct patient costs and increasing eligibility for patient assistance programs for uninsured and under-insured patients.
Continue reading »In an August 22, 2016, New York Times article, Tara Parker-Pope and Rachel Rabkin Peachman reported on the steep increase in the price of the EpiPen, a lifesaving injection device for people with severe allergies, and the outrage these price increases have caused with consumers and lawmakers.
Continue reading »How do we stay safe and keep our families safe when products we use are recalled for safety reasons? Safety recalls are very important for all of us. Rarely a week, or sometimes even a day, passes without news of some type of consumer product, medical product, medicine, automotive, or food recall.
Continue reading »Last week, the U.S. Food and Drug Administration (FDA) issued a Safety Communication advising that there are serious side effects associated with fluoroquinolone antibacterial drugs.
Continue reading »Essure is a permanent, implantable, birth control device for women, and was given approval back in 2002. Since that time, thousands of complaints have been submitted to the FDA. In September of 2015, the FDA held a hearing allowing stakeholders and other interested parties to testify before the September Advisory Committee. The FDA decided to take the following actions ...
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