FDA RECALL: Texas‑based Centric Compounding has recalled multiple lots of three injectable wellness products after identifying elevated endotoxin contamination, a toxin‑related risk that can trigger severe medical reactions, including anaphylactic shock and death. The FDA annonced the company’s voluntary recall on September 13, 2026.
The recall covers six lots of Glutathione 200 mg/mL, Myer’s Cocktail, and Tri‑Immune Boost, all packaged in 30 mL multidose vials and distributed nationwide, including direct‑to‑patient shipments. Because these products are commonly used in IV‑therapy and wellness clinics, the recall may affect residents in Brunswick and Columbus counties.
Centric Compounding reported nine adverse events consistent with endotoxin exposure, including fever, chills, chest pain, nausea, vomiting, headache, and malaise.
Recall product and lot numbers
- Glutathione 200 mg/mL Lots 062326:B, 070826:A, 072726:D
- Myer’s Cocktail Lots 070226:D, 072126:A
- Tri‑Immune Boost Lot 071626:B
The FDA warns that endotoxin contamination in injectable products can cause fever, hypotension, systemic inflammatory responses, anaphylactic shock, and death. Patients who received injections from the recalled lots should stop using the products immediately and contact a healthcare provider if symptoms occur.
Centric Compounding can be reached at 833.777.6664 or info@centriccompounding.com for recall questions.
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