Is this recall still active?

The FDA lists the recall as ongoing. The recall is still in progress.

Checked Oct 26, 2026

Not Yet ClassifiedDrug recallOngoing

Tri-Immune Boost (Glutathione: recall

Recalled by Centric Compounding LLC of Tomball, TX · FDA report 10/14/2026

Not an official recall notice and may be delayed. Confirm with the manufacturer or the agency.

Class: Not Yet Classified
Status: Ongoing
Recall started: 07/27/2026
Distribution: Nationwide

Reason for recall

Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.

Recalled product

Product: Tri-Immune Boost (Glutathione: 200 mg, Ascorbic Acid: 200 mg, Zinc: 2.5 mg), 30 mL vial, Rx only, Centric Compounding, 7447 Harwin Dr. Suite 111, Houston, TX 77036
Lot and code info: Lot #: 071626:B, Beyond Use Date: 8/30/26
Event ID: 99860
Initiated by: Voluntary: Firm initiated

Where it was distributed

USA Nationwide.

Nationwide

Recall timeline

07/27/2026Firm started the recall
10/14/2026Published in the FDA enforcement report

Frequently asked questions

Why was Tri-Immune Boost (Glutathione: recalled?: Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
Where was the recalled product sold?: USA Nationwide.
Is this recall still active?: The FDA lists the recall as ongoing. The recall is still in progress.

Source: U.S. Food and Drug Administration, openFDA enforcement report · Last updated 10/14/2026 · Do not rely on openFDA to make decisions regarding medical care

Recall at a glance

Class: Not Yet Classified
Status: Ongoing
Type: Drug
Reported: 10/14/2026

FDA enforcement report search

What recall classes mean

Class IMost serious: A reasonable chance that using or being exposed to the product will cause serious health problems or death.
Class IIModerate: Use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious harm is remote.
Class IIILow risk: Use of or exposure to the product is not likely to cause adverse health consequences.

Classes are assigned by the FDA based on the health hazard.

If you have a recalled product

Stop using or eating it. Check the lot number, UPC or date code against the recall.
Return it to the store or follow the firm's instructions for a refund, repair or disposal.
For medicines, talk to your pharmacist or doctor before stopping a prescription.
Report problems to the FDA through MedWatch or to the CPSC at SaferProducts.gov.

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About this data

Recalls: Recall information comes from NHTSA, FDA, USDA, CPSC and other agencies. A product, vehicle or lot may be affected even if it is not listed here, and listings may be delayed. Check the official recall notice and contact the manufacturer or dealer to confirm whether your item is included.

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