FDA recalls Guru Inc.'s Infla-650 Herbal Dietary Supplement due to undeclared acetaminophen, diclofenac, and phenylbutazone. Products may cause serious health risks if taken without FDA approval.
Marketed without an approved NDA/ANDA: FDA analysis found product to be tainted with undeclared acetaminophen, diclofenac, and phenylbutazone.
Guru Inc. is recalling Infla-650 Herbal Dietary Supplements because they contain undeclared ingredients that the FDA found unsafe. These supplements were sold with a label claiming they were approved, but they actually contain harmful substances that could cause serious health issues.
The supplement contains undeclared acetaminophen, diclofenac, and phenylbutazone, which are drugs that can cause serious health problems like liver damage, kidney failure, or other severe reactions. These ingredients were not approved by the FDA and were not disclosed on the product label.
Anyone who purchased the Infla-650 Herbal Dietary Supplement from Guru Inc. in the U.S. or India. People taking the supplement regularly are most at risk due to the potential for serious health effects.
Look for the Infla-650 Herbal Dietary Supplement, 700mg, packaged in pouches with 60 capsules. The product was distributed by Guru Inc. in the U.S. and India, with batch number IN-032 and expiration date 11/30/2027.
Immediately stop taking the Infla-650 Herbal Dietary Supplement as it contains undeclared drugs that could cause serious health issues.
The FDA found that the product contains undeclared acetaminophen, diclofenac, and phenylbutazone, which are drugs not approved for use in dietary supplements.
Taking this supplement could lead to serious health problems such as liver damage, kidney failure, or other severe reactions due to the presence of undeclared drugs.
Check for the Infla-650 Herbal Dietary Supplement, 700mg, packaged in pouches with 60 capsules. The product was distributed by Guru Inc. with batch number IN-032 and expiration date 11/30/2027.
We’ve drafted a message you can send Guru Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-0666-2024 — Guru Inc. Guru Inc. Hello, I own a Guru Inc. that is covered by recall D-0666-2024 from Guru Inc.. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
