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Lower risk Food recall · FDA · Published February 25, 2026

WeiKFiELD Custard Powder Recalled for Labeling Error

Weikfield Foods recalls WeiKFiELD Custard Powder Kesar Pista (Lot 118) due to incorrect ingredient labeling. Check your pantry.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #H-0911-2026FoodWeiKFiELD ›
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Contact the company

Recalling firmWeikfield Foods Pvt. Ltd.Weik Field Foods Pvt. Ltd. Gat No. 323/331, Village - Bakori, Taluka - Haveli · Pune, India
✎ GovInfoNow plain-language explainer

Weikfield Foods Pvt. Ltd. is recalling one lot of WeiKFiELD Custard Powder Kesar Pista because the label incorrectly lists 'Pista' instead of the standard American term 'Pistachio.' This is a Class III recall, which typically involves products that are unlikely to cause adverse health consequences but violate labeling regulations. The company has not provided a specific remedy or return instructions in this record. Read more at govinfonow.com/recall/6698-weikfield-custard-powder-recalled-for-labeling-error.

Source Summary by GovInfoNow · govinfonow.com/recall/6698-weikfield-custard-powder-recalled-for-labeling-error · Updated October 9, 2026 · Official notice: FDA #H-0911-2026

Cite this page

“WeiKFiELD Custard Powder Recalled for Labeling Error.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/6698-weikfield-custard-powder-recalled-for-labeling-error. Based on FDA recall #H-0911-2026.

The FDA announced on Feb. 25, 2026, that Weikfield Foods Pvt. Ltd. voluntarily recalled WeiKFiELD Custard Powder Kesar Pista due to mislabeling of the pistachio ingredient. The agency classified the recall as Class III.

How to tell if you have it

  • Brand: WeiKFiELD
  • Product: Custard Powder Kesar Pista
  • Size: Net Wt. 300g (10.6 OZ.), Poly Jar
  • Lot No.: 118

The hazard

The FDA said the ingredient 'Pista' declared on the label should be corrected to the standard American nomenclature, Pistachio. The product was distributed to Iowa, Ohio, North Carolina, New Jersey, and Illinois.

Context

GovInfoNow's records show other recent recalls of similar products include Albertsons Cake Pistachio Dessert 1CT Recall (2026-05-06), Albertsons Cake Boston Creme Dubai 5in Recall (2026-05-06), and Albertsons Croissants Dubai Chocolate 2CT Recall (2026-05-06).

How to tell if you have this one

Check your pantry for WeiKFiELD Custard Powder Kesar Pista in a poly jar, Net Wt. 300g (10.6 OZ.). Specifically look for Lot No. 118 on the packaging. The product was distributed to Iowa, Ohio, North Carolina, New Jersey, and Illinois.

  • Brand
    WeiKFiELD
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Your Product

    Verify if you have WeiKFiELD Custard Powder Kesar Pista with Lot No. 118.

  2. Review Labeling

    Note that the label uses 'Pista' instead of 'Pistachio,' which is the subject of this recall.

Where it went and when

Where it was distributed

Distributed in 4 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: yesIAIndiana: not listedINOhio: yesOHPennsylvania: not listedPANew Jersey: yesNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “The adulterated product was distributed to the following states: Iowa, Ohio, North Carlina, New Jersey, & Illinois” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Illinois, Iowa, New Jersey, Ohio.

Recall timeline

FDA terminated this recall 5 months after the firm started it.

1. Firm started the recall: Feb 25, 202612. FDA classified it Class III: Jun 8, 202623. Published in FDA’s Enforcement Report: Jun 17, 202634. FDA terminated the recall: Jul 23, 202642026
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

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.

  • Official source: FDA Recall #H-0911-2026 (February 25, 2026)
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA