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Drug Recall Community & Access

Published September 13, 2026

DRUG RECALL HEALTHCARE, MENTAL HEALTH & AGING

Check the vial: six Centric Compounding injectable lots have been recalled.

Centric Compounding says the affected 30 mL vials were delivered nationwide to patients at home and to prescribers. That makes this an exact-match check—not a warning about every glutathione injection, Myer's Cocktail or Tri-Immune Boost product.

The Rockland Edit drug-recall card listing six recalled Centric Compounding lots across Glutathione, Myer's Cocktail and Tri-Immune Boost, with stop-use and discard instructions
Drug-recall identification card by The Rockland Edit, based on the FDA-posted Centric Compounding announcement. It is an original editorial graphic—not a product photograph, vial label or medical instruction.

Match the product, lot and beyond-use date

  • Glutathione 200 mg/mL: lot 062326:B, BUD 8/7/26; lot 070826:A, BUD 8/22/26; or lot 072726:D, BUD 9/25/26.
  • Myer's Cocktail: lot 070226:D, BUD 8/16/26; or lot 072126:A, BUD 9/4/26.
  • Tri-Immune Boost: lot 071626:B, BUD 8/30/26.
  • Container: 30 mL multidose injectable vial.

If every detail matches

  1. Stop using the vial and discard it, as the company recall directs.
  2. Contact Centric Compounding about a replacement at 833-777-6664 or info@centriccompounding.com. The company lists phone hours Monday through Friday, 9 a.m.–5 p.m. Central Time.
  3. If you experienced a problem that may be related to the product, contact a physician or healthcare provider. Call 911 for a medical emergency.

Patients and healthcare professionals may also report adverse reactions or product-quality problems through the FDA's MedWatch program ↗.

Why the company recalled the lots

The FDA-posted company announcement says the products were compounded with a glutathione active pharmaceutical ingredient that contained elevated endotoxin levels. Centric Compounding's risk statement says injectable products with elevated endotoxin have a reasonable probability of causing significant medical events, including fever, low blood pressure, inflammatory reactions, anaphylactic shock and death. That is the company's stated risk assessment; the notice does not say that every recalled vial contains the same endotoxin level.

The company reports nine complaints involving fever, chills, chest pain, nausea or vomiting, headache and/or malaise. The announcement does not say that every complaint was independently confirmed as caused by a recalled vial.

What nationwide delivery does—and does not—confirm

The announcement says the products were delivered nationwide to patients through home delivery and to prescribers. A Rockland recipient is therefore possible without a local retail sale. The public notice does not identify individual recipients or locations, and The Rockland Edit has not confirmed a Rockland patient, prescriber, delivery, complaint, illness or death.

This is separate from the earlier glutathione recall

This notice concerns Centric Compounding and six product-lot combinations. It does not expand the one-lot Optimal Balance Pharmacy recall published in August. Readers checking that separate product can use The Rockland Edit's Optimal Balance lot guide.

The useful version is exact: match Centric Compounding, the product name, 30 mL vial, lot and beyond-use date. If every detail matches, stop using and discard the vial, contact the company about replacement and contact a healthcare provider about any potentially related problem.

Primary source: FDA-posted Centric Compounding company announcement ↗, dated September 11 and published by FDA September 13, 2026. Product identifiers, nationwide delivery, consumer instructions, contact information, complaint count and recall status checked September 13, 2026, at 4:56 p.m. EDT. FDA posts company announcements as a public service and does not endorse the product or company. This service guide is not individualized medical advice.

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