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FDA recall record

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

Recall H-0911-2026Class IIITerminatedFebruary 25, 2026

FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.

FDA listed a termination date of July 23, 2026. openFDA does not treat this as a live recall-status tracker.

Product described in an FDA recall

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

Reason

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

Products involved

Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.

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

Code information listed by FDA

Lot No. 118

Distribution and firm information

Recalling firm listed by FDA: Weikfield Foods Pvt. Ltd.

Firm location listed by FDA: Pune, N/A, India

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

Product quantity listed by FDA: 8 cases (of 24 units each)

Source

Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.

Official FDA openFDA food enforcement record

Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.