CLASS I Food recall · Reported 26 Feb 2025 · FDA Enforcement Report

Zaarah Herbals Shatavari Powder recalled by New York Wholesale Group

New York Wholesale Group is recalling Zaarah Herbals Shatavari Powder, distributed in California, Connecticut, New Jersey, New York. The recall was initiated on 27 Jan 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBatch No: SR 04 Mfd. Date: JULY/2022.
Quantity recalled1584 pcs

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0567-2025
FDA event ID
96177
Recalling firm
New York Wholesale Group, Hicksville, NY
Classification
Class I
Status
Terminated
Recall initiated
27 Jan 2025
FDA classified
19 Feb 2025
Reported
26 Feb 2025
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Lead & Heavy Metals
Product category
Herbal Supplements

Timeline

27 Jan 2025Recall initiated by company
19 Feb 2025Classified by FDA+23 days
26 Feb 2025Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product contains elevated levels of lead - 6.50 mg/kg (ppm)

Lead and other heavy metals accumulate in the body. Children are most at risk; even low levels can affect development.

Product as listed by the FDA

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

Where it was distributed

NY, NJ, CT, CA

CaliforniaConnecticutNew JerseyNew York

Questions about this recall

Why was it recalled?

Product contains elevated levels of lead - 6.50 mg/kg (ppm)

Which lots are affected?

Batch No: SR 04 Mfd. Date: JULY/2022.

Where was it sold?

NY, NJ, CT, CA

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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