Recall of ZAARAH HERBALS Shatavar Powder due to elevated lead levels (6.50 mg/kg) in product. Consumers should stop using affected items.
Product contains elevated levels of lead - 6.50 mg/kg (ppm)
New York Wholesale Group is recalling ZAARAH HERBALS Shatavar Powder because it contains elevated lead levels. This poses a health risk, especially for children and pregnant women who may be exposed through consumption.
The product contains 6.50 mg/kg of lead, which is above safe levels. Lead exposure can cause serious health issues, particularly in children and pregnant women, including developmental delays and neurological damage.
Anyone who purchased this product from a retailer in the U.S. is affected. Pregnant women and young children are at higher risk due to lead exposure.
Look for the product labeled 'ZAARAH HERBALS brand SHATAVARI POWDER; 100% ASPARAGUS RACEMOSUS; (Supports Female Reproductive System); Supreme Fine' in a clear bottle with gold lid. The UPC is 63502899940 and batch number SR 04 with a manufacturing date of July 2022.
Immediately stop using the product as it contains elevated lead levels that can cause serious health risks.
No, the product contains elevated lead levels (6.50 mg/kg) which can cause serious health risks, especially for children and pregnant women.
Check for the product labeled 'ZAARAH HERBALS brand SHATAVARI POWDER; 100% ASPARAGUS RACEMOSUS; (Supports Female Reproductive System); Supreme Fine' in a clear bottle with gold lid. The UPC is 63502899940 and batch number SR 04 with a manufacturing date of July 2022.
Immediately stop using the product and contact New York Wholesale Group for a refund or replacement.
We’ve drafted a message you can send ZAARAH HERBALS to request your refund or repair — edit it as you like.
Subject: Recall F-0567-2025 — ZAARAH HERBALS ZAARAH HERBALS Hello, I own a ZAARAH HERBALS that is covered by recall F-0567-2025 from ZAARAH HERBALS. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
