Class IIITerminatedVoluntary: Firm initiated
Weikfield Foods Pvt. Ltd.: food recall H-0911-2026
Weikfield Foods Pvt. Ltd. of Pune, N/A recalled 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. The FDA listed it as Class III in its Enforcement Report dated Jun 17, 2026; distribution: Iowa, Illinois, New Jersey, Ohio.
Record status as published: Terminated (terminated Jul 23, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- WeiKFiELD Custard Powder Kesar Pista, Net Wt. 300g (10.6 OZ.), Poly Jar , 24 units per outer case.
- Product quantity
- 8 cases (of 24 units each)
- Reason for recall
- The ingredient, Pista, currently declared on our label should be corrected to the standard American nomenclature, Pistachio.
- Codes, lots and dates on the package
- Lot No. 118
- Distribution pattern
- The adulterated product was distributed to the following states: Iowa, Ohio, North Carlina, New Jersey, & Illinois
- Recalling firm
- Weikfield Foods Pvt. Ltd., Pune, N/A, India
- Classification
- Class III — the FDA uses this class for a situation in which using or being exposed to the product is not likely to cause adverse health consequences.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Telephone
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Feb 25, 2026 |
| Classified by the FDA | Jun 8, 2026 |
| Published in the Enforcement Report | Jun 17, 2026 |
| Terminated | Jul 23, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0911-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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