US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Jun 26, 2024 (2 years ago)

Infla-650 Herbal Dietary Supplement, 700mg, packaged in pouches containing 60 capsules…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Marketed without an approved NDA/ANDA: FDA analysis found product to be tainted with undeclared acetaminophen, diclofenac, and phenylbutazone.

What was recalled

Infla-650 Herbal Dietary Supplement, 700mg, packaged in pouches containing 60 capsules, Distributed by: Guru Inc., 4370 Lawrenceville Hwy NW, P.O. Box 2204, Lilburn, GA 30047-1100, USA. Ph.: 872 216 1566, http://www.dalayurevda.com, Made in India, UPC: 042535355019

Recalling firm
Guru Inc.
Origin
GA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0666-2024

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.