Class ITerminatedVoluntary: Firm initiated

NEW YORK WHOLESALE GROUP: food recall F-0567-2025

NEW YORK WHOLESALE GROUP of Hicksville, NY recalled ZAARAH HERBALS brand SHATAVARI POWDER; 100% ASPARAGUS RACEMOSUS; (Supports Female Reproductive System); Supreme Fine… Reason: Product contains elevated levels of lead - 6.50 mg/kg (ppm). The FDA listed it as Class I in its Enforcement Report dated Feb 26, 2025; distribution: California, Connecticut, New Jersey, New York.

Record status as published: Terminated (terminated Jul 21, 2026). openFDA data last updated Oct 21, 2026.

Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.

Recall details

Product
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
Product quantity
1584 pcs
Reason for recall
Product contains elevated levels of lead - 6.50 mg/kg (ppm)
Codes, lots and dates on the package
Batch No: SR 04 Mfd. Date: JULY/2022.
Distribution pattern
NY, NJ, CT, CA
Recalling firm
NEW YORK WHOLESALE GROUP, Hicksville, NY
Classification
Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Voluntary or mandated
Voluntary: Firm initiated
How the firm first notified customers
Press Release

Dates

EventDate
Recall initiated by the firmJan 27, 2025
Classified by the FDAFeb 19, 2025
Published in the Enforcement ReportFeb 26, 2025
TerminatedJul 21, 2026

Other recalls by NEW YORK WHOLESALE GROUP

  • F-0724-2025 · Apr 30, 2025 · Class I — Products contain elevated levels of Lead (Pb): 88.038 ppm
  • F-0723-2025 · Apr 30, 2025 · Class I — Products contain elevated levels of Lead (Pb): 6.504 ppm
  • F-0722-2025 · Apr 30, 2025 · Class I — Products contain elevated levels of Lead (Pb): 3.688 ppm
  • F-0721-2025 · Apr 30, 2025 · Class I — Products contain elevated levels of Lead (Pb): 3.231 ppm and Arsenic (As): 0.958 ppm;

All food recall records

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Sources

  • U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0567-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
  • Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.