Fresh Recalls

FDAClass III · Food · Recall H-0911-2026 · Recalled June 17, 2026

WeiKFiELD Custard Powder Kesar Pista recall — Weikfield Foods Pvt. Ltd.

Agency report date: June 17, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
WeiKFiELD Custard Powder Kesar Pista
Company / brand
Weikfield Foods
Lot / serial / date codes
Lot No. 118
Distribution
The adulterated product was distributed to the following states: Iowa, Ohio, North Carlina, New Jersey, & Illinois
Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

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

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class III: not likely to cause adverse health consequences.

Affected product: WeiKFiELD Custard Powder Kesar Pista

3. Open the official notice or contact

Official recall ID
H-0911-2026
Brand
Weikfield Foods
Classification
Class III
Units affected
8 cases (of 24 units each)
Recall status
Terminated
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Pune, N/A, India
Firm address
Weik Field Foods Pvt. Ltd. Gat No. 323/331, Village - Bakori, Taluka - Haveli, N/A

Identifying details (verbatim from the notice)

Product codes / lots
Lot No. 118
Distribution
The adulterated product was distributed to the following states: Iowa, Ohio, North Carlina, New Jersey, & Illinois
Firm notified the public via
Telephone
FDA event ID
98850
Recall initiated
February 25, 2026
FDA classified
June 8, 2026
FDA report date
June 17, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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