ZAARAH HERBALS brand SHATAVARI POWDER; 100% ASPARAGUS RACEMOSUS; (Supports Female Reproductive System); Supreme Fine Pow
Summary
The FDA issued a Class I for ZAARAH HERBALS brand SHATAVARI POWDER; 100% ASPARAGUS RACEMOSUS; (Supports Femal by NEW YORK WHOLESALE GROUP. Reason: Product contains elevated levels of lead - 6.50 mg/kg (ppm).
Details
Source
Food Recall
External ID
F-0567-2025
Action Date
2025-02-26
Status
Ongoing
Category
food
Product Description
ZAARAH HERBALS brand SHATAVARI POWDER; 100% ASPARAGUS RACEMOSUS; (Supports Female Reproductive System); Supreme Fine Powder 100g (3.5 oz); Manufactured by FALCON SYSTEM OF AYUREVEDIC PRODUCTS Auto Nagar, Belgaum, Karnataka 590015 (INDIA); Manufactured for: ZAARAH HERBALS, USA; packaged in clear bottle with gold lid; UPC: 63502899940
Lot/Code Info: Batch No: SR 04 Mfd. Date: JULY/2022.
Quantity Affected: 1584 pcs
Reason for Recall
Product contains elevated levels of lead - 6.50 mg/kg (ppm)
Distribution
NY, NJ, CT, CA
Type: Voluntary: Firm initiated
Recall Initiated: 2025-01-27
Company
Hicksville, NY
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 37 food recalls issued in the same week, part of 204 food-related FDA actions this month.
NEW YORK WHOLESALE GROUP has 5 FDA actions in our database, including 5 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (NEW YORK WHOLESALE GROUP) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does NEW YORK WHOLESALE GROUP have FDA actions?
NEW YORK WHOLESALE GROUP has 5 FDA actions in our database, including 5 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0567-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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