WeiKFiELD Custard Powder Kesar Pista Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Weikfield Foods Pvt. Ltd. is recalling 8 cases of WeiKFiELD Custard Powder Kesar Pista due to an incorrect ingredient name on the label.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on July 27, 2026 and geographically references Iowa, Ohio, North Carolina, New Jersey, Illinois. Its severity classification of "low" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Food.
What Happened
Weikfield Foods Pvt. Ltd. initiated a voluntary recall because the ingredient listed as "Pista" on the label should be corrected to the standard American nomenclature "Pistachio."
Which Products Are Affected
The recall involves WeiKFiELD Custard Powder Kesar Pista, Net Wt. 300g (10.6 OZ.), Poly Jar, 24 units per outer case, Lot No. 118. A total of 8 cases were distributed to Iowa, Ohio, North Carolina, New Jersey, and Illinois. The recall number is H-0911-2026.
What You Should Do
Consumers in the affected states should check purchased products for Lot No. 118.
Why This Matters
This is a Class III recall involving a labeling nomenclature correction with no reported health risks.
Source
FDA recall H-0911-2026
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (749 characters here).
Similar severity timing
Same severity (low) notices issued closest in time to July 27, 2026.
Frequently Asked Questions
Common questions about this FDA recall.