Riddhi USA Dietary Supplements Recall: Full Product Recall
Riddhi USA Inc. is recalling all dietary supplements they manufactured and distributed due to a legal requirement under a Consent Decree. No specific product details or safety risks are mentioned in the recall notice.
Recall notice
Per order of the Consent Decree, firm is recalling all dietary supplements.
Contact the company
What happened, in plain English
Riddhi USA Inc. is recalling all dietary supplements they made and distributed. This recall is required by a legal order, but the notice doesn't specify any safety risks or product details to check. Read more at govinfonow.com/recall/19230-riddhi-usa-dietary-supplements-recall-full-product-recall.
Source Summary by GovInfoNow · govinfonow.com/recall/19230-riddhi-usa-dietary-supplements-recall-full-product-recall · Updated October 7, 2026 · FDA enforcement record: FDA #F-1172-2018
Cite this page
“Riddhi USA Dietary Supplements Recall: Full Product Recall.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19230-riddhi-usa-dietary-supplements-recall-full-product-recall. Based on FDA recall #F-1172-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1172-2018%22&limit=1).
Why it’s dangerous
The recall is based on a legal requirement from a Consent Decree, not on a safety hazard. The notice does not describe any risk to health or safety.
Who’s affected
All owners of dietary supplements made by Riddhi USA Inc. are affected. There is no specific group identified as being at higher risk.
How to tell if you have this one
This recall covers all dietary supplements manufactured and distributed by Riddhi USA Inc. within their expiry dates. No specific product names or model numbers are listed.
- Brand
Riddhi USA- Category
Food
What to do — step by step
Check Product Details
Review the product label for the manufacturer name 'Riddhi USA Inc.' and the expiry date.
Where it went and when
Where it was distributed
Distributed in 3 states.
FDA distribution: “NY, DE, NJ” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Delaware, New Jersey, New York.
Recall timeline
FDA terminated this recall 7 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #F-1172-2018 (April 10, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1172-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.