New York Wholesale Group food recall: ZAARAH HERBALS brand SHATAVARI POWDER
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Terminated
- Event ID
- 96177
- Recall initiated
- Jan 27, 2025
- Classified by FDA
- Feb 19, 2025
- Posted in Enforcement Report
- Feb 26, 2025
- Terminated
- Jul 21, 2026
- Recalling firm
- NEW YORK WHOLESALE GROUP
- Firm location
- Hicksville, NY, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Press Release
- Products in this event
- 1
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Product contains elevated levels of lead - 6.50 mg/kg (ppm)
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Jan 27, 2025. FDA classified it 23 days later, on Feb 19, 2025. Distribution reported by FDA: NY, NJ, CT, CA NEW YORK WHOLESALE GROUP has 2 recalls in our records.
Recalled products (1)
F-0567-2025 Class I Terminated
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
Codes / lots: Batch No: SR 04 Mfd. Date: JULY/2022.
Quantity: 1584 pcs
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 96177
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.