Infla-650 Herbal Dietary Supplement — Class II drug recall D-0666-2024
Ongoing recall by Guru Inc., reported 2024-10-02, distributed nationwide. Marketed without an approved NDA/ANDA: FDA analysis found product to be tainted with undeclared acetaminophen,
| Recall number | D-0666-2024 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Guru Inc., Lilburn, GA, United States |
| Recall initiated | 2024-06-26 |
| Classified | 2024-09-23 |
| Reported by FDA | 2024-10-02 |
| Distributed | Nationwide (US) |
| Reason classes | undeclared allergen, unapproved product |
| UPC / GTIN / UDI-DI | 00042535355019 |
| Lot numbers | IN-032 |
| Expiration dates | 2027-11-30 |
Product
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
Reason for recall
Marketed without an approved NDA/ANDA: FDA analysis found product to be tainted with undeclared acetaminophen, diclofenac, and phenylbutazone.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0666-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.