More than 25 people in at least four states got sick after compounded glutathione injections and IVs made from a supplement-grade ingredient, and the story is back in the news this weekend. (1)(2) WHAT IT IS Glutathione is a small peptide (three amino acids) that wellness clinics sell as IV drips and shots for "detox," immunity and energy. In July 2026, Texas health officials alerted the CDC to patients who got sick after IV glutathione at an outpatient wellness clinic. CDC and FDA have been investigating since. (1) WHAT THEY FOUND • CDC counts more than 25 cases in Texas, Washington, Florida and New York. At least 3 people were hospitalized, all after IV glutathione. One was critically ill, needed intensive care, and was treated for shock and abnormal blood clotting. No deaths are listed. (1) • FDA said it knew of at least 30 patients with adverse events after IV glutathione. The ingredient traced back to one supplier (Medisca, lot 229536) and was labeled "dietary supplement grade." (3) • Three Texas compounding pharmacies recalled products for elevated endotoxin: Victory Medical Center Pharmacy, Optimal Balance Pharmacy and Centric Compounding. (1)(4)(5) • Centric's recall also covered Myer's Cocktail and Tri-Immune Boost vials made with the same ingredient, shipped nationwide by home delivery. It received 9 reports of fever, chills, chest pain, nausea or vomiting, headache and malaise. (5) • Victory's reports included fever, chills, severe headache, vomiting, rapid heart rate, blood pressure changes and injection-site reactions. (4) HOW IT WORKS Endotoxin is a bacterial contaminant. Once injected, it can set off a strong inflammatory reaction: fever, chills, body aches, low blood pressure and, at worst, shock. (1)(5) The core problem was the raw material. FDA's position is that every ingredient in an injectable has to be made to standards that fit that route, and that testing the finished vial is not a substitute for building quality in from the start. (3)(6)