FDA Recall United States Completed Historical recordClass I
NEW YORK WHOLESALE GROUP
- Product
- Zaarah Herbals brand Rasayan Churan; packaged in 100g clear…
- Published
- April 30, 2025
- Distribution
- Multiple states
NEW YORK WHOLESALE GROUP Recall: Product contains elevated levels of lead - 6.50 mg/kg (ppm)
United States
CompletedClass I
- Company
- NEW YORK WHOLESALE GROUP
- Product
- ZAARAH HERBALS brand SHATAVARI POWDER; 100% ASPARAGUS RACEMO…
- Recall date
- January 27, 2025
- Source
- FDA
Reason for recall
Product contains elevated levels of lead - 6.50 mg/kg (ppm)
- - Recall initiated
- - Reported by source
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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 | 63502899940 | 1584 pcs | Batch No: SR 04 Mfd. Date: JULY/2022. |
Distribution
- NY
- NJ
- CT
- CA
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0567-2025
- Event ID
- 96177
- Status
- Completed
- Classification
- Class I
- Company
- NEW YORK WHOLESALE GROUP
- 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
- Quantity
- 1584 pcs
- Reason
- Product contains elevated levels of lead - 6.50 mg/kg (ppm)
- Recall initiation date
- January 27, 2025
- Report date
- February 26, 2025
- Classification date
- Not published in this source record
- Termination date
- Not terminated as of this source record
- Distribution pattern
- NY, NJ, CT, CA
- UPC, lot, and code information
- UPC 63502899940; Batch No: SR 04 Mfd. Date: JULY/2022.
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Press Release
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: NEW YORK WHOLESALE GROUP
Other recalls from NEW YORK WHOLESALE GROUP
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FDA Recall United States Completed Historical recordClass I
NEW YORK WHOLESALE GROUP
- Product
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- Published
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- Distribution
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A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| New York | 1 |
| New Jersey | 1 |
| Connecticut | 1 |
| California | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Completed." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
