The Recall Desk
SevereFDA (Food)·F-1172-2018·Announced 2018-05-09

Riddhi USA Inc. Recalls All Dietary Supplements Under Consent Decree

Riddhi USA Inc. is recalling all dietary supplements it manufactures and distributes in New York, Delaware, and New Jersey pursuant to a Consent Decree.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The agency classification is FDA Class II, which corresponds to a score of 4 (Severe) per the rubric, as it involves a reasonable probability of temporary or medically reversible adverse health consequences.

Plain-English summary

Riddhi USA Inc. is recalling all dietary supplements manufactured and distributed by the company. This action is being taken per the order of a Consent Decree. The total quantity of affected products is unknown, and all items are within their expiration dates.

The recall covers distribution in New York, Delaware, and New Jersey. The source text does not specify the exact reason for the Consent Decree or list specific product names, lot numbers, or reported illnesses.

Consumers who have purchased these products should stop using them and contact the recalling firm for further instructions.

The recalled product

Product
All dietary supplements manufactured and distributed by Riddhi USA Inc.
Manufacturer
Riddhi USA Inc.
Category
Food — Dietary Supplements
Hazard

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • All within expiry.

Distribution

Distributed in 3 states:

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