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Ongoing FDAEvent 99860 (1 month ago)

Centric Compounding Glutathione, Myers Cocktail and Tri-Immune Boost Injections

Glutathione, Myer's Cocktail, and Tri-Immune Boost injectable vials may contain elevated endotoxin levels, which could cause significant medical events.

What to do

What happened

FOR IMMEDIATE RELEASE – 9/9/2026 – Houston, Texas, Centric Compounding is voluntarily recalling 6 lots of Glutathione 200mg/mL, Myer’s Cocktail, and Tri-Immune Boost injectable vials to the consumer level. Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.

These products were distributed Nationwide to patients via home delivery and delivery to prescribers.

From the FDA notice.

What to do

If a code on your package matches:

  1. Consumers that have Glutathione, Myer’s Cocktail, and Tri-Immune Boost which is being recalled should stop using.
  2. Discard any affected vials.
  3. Consumers with questions regarding this recall can contact Centric Compounding by phone at 833-777-6664 or info@centriccompounding.com on Monday through Friday from 9am to 5pm CST.
  4. Contact your physician or healthcare provider if you have experienced any problems that may be related to taking or using this drug product.

Is yours affected?

3 products

Match your product and all the details in one listed combination.

  1. Tri-Immune Boost 30mL vial

    Lot code
    • 071626:B
    Beyond use date
    8/30/26
  2. Glutathione 200mg/ml 30mL vial

    1. Lot code
      • 062326:B
      Beyond use date
      8/7/26
    2. Lot code
      • 070826:A
      Beyond use date
      8/22/26
    3. Lot code
      • 072726:D
      Beyond use date
      9/25/26
  3. Myer's Cocktail 30mL vial

    1. Lot code
      • 070226:D
      Beyond use date
      8/16/26
    2. Lot code
      • 072126:A
      Beyond use date
      9/4/26

Details

Company began the recall
Sold in

These products were distributed Nationwide to patients via home delivery and delivery to prescribers.

Event ID
99860
Company
Centric Compounding LLC
  1. Company began the recall

  2. Announced by the company

  3. Listed on Recall Canary

  4. Added to FDA's Enforcement Report

  5. Summary updated

  6. In FDA's weekly enforcement report

Summary by Recall Canary, written with AI · summary updated Oct 7, 2026 · primary source: U.S. Food and Drug Administration