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FDA source record Class III Ongoing

WeiKFiELD Custard Powder Kesar Pista, Net Wt. 300g (10.6 OZ.), Poly Jar , 24 units per outer case.

Recall Date: 2026-02-25 Recalling Firm: Weikfield Foods Pvt. Ltd. Record Ref: H-0911-2026

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns WeiKFiELD Custard Powder Kesar Pista, Net Wt. 300g (10.6 OZ.), Poly Jar , 24 units per outer case. and names Weikfield Foods Pvt. Ltd. as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: Weikfield Foods Pvt. Ltd.
  • Classification: Class III
  • Status: Ongoing
  • Recall date: 2026-02-25
Best identifiers to check for a FDA record

Compare UPC/GTIN, lot or batch code, package size, flavor or variety, and any best-by/use-by date listed in the notice.

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Product Description & Identification

WeiKFiELD Custard Powder Kesar Pista, Net Wt. 300g (10.6 OZ.), Poly Jar , 24 units per outer case.

Reason for Recall / Hazard Identified

The ingredient, Pista, currently declared on our label should be corrected to the standard American nomenclature, Pistachio.

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

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Distribution & Affected States

The adulterated product was distributed to the following states: Iowa, Ohio, North Carlina, New Jersey, & Illinois

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:12 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
H-0911-2026
Indexed update
2026-08-09 21:59:12 UTC
Official source
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