Centric Compounding Recall: Glutathione, Myer’s Cocktail & Tri-Immune Vials Pulled for Endotoxin Risks
Centric Compounding LLC has initiated a voluntary nationwide recall of six lots of its compounded Glutathione 200 mg/mL, Myer’s Cocktail and Tri-Immune Boost injectables after internal testing revealed elevated endotoxin levels. Patients infused with the affected vials face a higher risk of fever, hypotension, systemic inflammatory response, anaphylactic shock or—even in rare cases—death. Discontinue use of the recalled vials immediately and dispose of them safely.
Why the Centric Compounding Injectables Are Being Recalled
The recalled batches were compounded with a Glutathione active pharmaceutical ingredient (API) tainted by elevated endotoxin levels. Endotoxins—components of the cell walls of gram-negative bacteria—can trigger severe immune reactions when introduced directly into the bloodstream.
Recalled Centric Compounding Lot Numbers
| Product | Lot # | Beyond-Use Date |
|---|---|---|
| Glutathione 200 mg/mL 30 mL vial | 062326:B | 08/07/26 |
| Glutathione 200 mg/mL 30 mL vial | 070826:A | 08/22/26 |
| Glutathione 200 mg/mL 30 mL vial | 072726:D | 09/25/26 |
| Myer’s Cocktail 30 mL vial | 070226:D | 08/16/26 |
| Myer’s Cocktail 30 mL vial | 072126:A | 09/04/26 |
| Tri-Immune Boost 30 mL vial | 071626:B | 08/30/26 |
Sources
Immediate Consumer Action Steps
- Verify the lot number on any Centric Compounding Glutathione, Myer’s Cocktail or Tri-Immune Boost vial in your possession.
- If it matches a recalled lot, stop using the product immediately.
- Safely discard the vial or arrange a replacement with Centric Compounding.
- Contact your healthcare provider if you experience fever, chills, chest pain, nausea, headache, malaise or other unusual symptoms.
- Report adverse events to FDA MedWatch:
How to Obtain a Centric Compounding Refund or Replacement
The company is emailing affected customers and offering replacements. To initiate the process:
- Call 833-777-6664 (Mon–Fri, 9 a.m.–5 p.m. CST)
- Email info@centriccompounding.com
Nationwide Distribution Scope
The recalled vials were shipped throughout the United States directly to patients and to healthcare providers’ offices.
Recall Timeline
- Recall initiated by company: September 9, 2026
- Company announcement: September 11, 2026
- FDA public posting: September 13, 2026
FAQ: Centric Compounding Endotoxin Recall
1. Which Centric Compounding products are affected by the recall?
Six lots of Glutathione 200 mg/mL, Myer’s Cocktail and Tri-Immune Boost 30 mL multidose vials.
2. What health risks do Centric Compounding endotoxin-tainted injectables pose?
Potential reactions include fever, low blood pressure, inflammatory response, anaphylactic shock and, in severe cases, death.
3. Where is the lot number printed on my Centric Compounding vial?
The lot number appears on the vial’s label, typically near the expiration or beyond-use date.
4. Will Centric Compounding refund or replace my recalled product?
Yes. Contact the company by phone or email to arrange a complimentary replacement; then dispose of the recalled vial safely.
5. I used a recalled Centric Compounding product and feel ill—what should I do?
Seek immediate medical attention and inform your provider that you used a recalled Centric Compounding injectable. Report the event to FDA MedWatch as well.
6. Is the Centric Compounding recall FDA-approved or mandatory?
The recall is voluntary but is being conducted with the full knowledge and oversight of the U.S. Food and Drug Administration.