Dixit Foods, Pohe, Net Wt. 110 g, Ingredients: Rice Flakes, Groundnuts, Edible Sunflower…
Bondsforever, Inc dba Shastha Foods recalled this product and the FDA reported the enforcement action on 21 May 2025 as Class II. The recall was initiated by the firm. Undeclared allergens (milk and/or peanuts).
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- Dixit Foods, Pohe, Net Wt. 110 g, Ingredients: Rice Flakes, Groundnuts, Edible Sunflower oil, Sugar, Salt, Green Chilli, Asafoetida, Curry Leaves, Mustard seeds, Turmeric Powder etc, Allergen Information: May contain Peanuts, Treenuts, Wheat, Sesame, Mustard
- Reason for recall
- Undeclared allergens (milk and/or peanuts).
- Recalling firm
- Bondsforever, Inc dba Shastha Foods
- Firm location
- San Jose, California, United States
- Classification
- Class II
- Status
- Ongoing
- Recall number
- F-0809-2025
- Quantity
- 300 packages
- Distribution
- CA, UT, WA
- Initiated
- 8 May 2025
- Reported by FDA
- 21 May 2025
- Firm notified by
- Letter
- Product codes
- UPC Code: 8908010443010 Batch Number: 04 Best By Date(s): September 10th 2025
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This is one of 2 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 2 separate recalls, which almost every published figure does, overstates it by a factor of 2. All 2 of them are listed on this page.
- This recall has no termination date on the record, so as published it had not been terminated under 21 CFR 7.55.
- The distribution pattern names 3 states, and the FDA published the enforcement report 13 days after the firm began the recall.
- Nuts and seeds carry both hazards at once: they are a major allergen in their own right, and as a low-moisture food they hold Salmonella for months without supporting its growth, which is why a nut butter recall can trace to a lot pressed a year earlier.
Named in the distribution pattern: California, Utah, Washington. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
What this recall was for
Undeclared allergens
An undeclared allergen recall means a food contained one of the major allergens and the label did not say so, either because the wrong label was applied or because an ingredient carried an allergen nobody traced.
A preventive controls plan covers an undeclared allergen under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.
- 21 CFR 117.135(c)(2)
- Food allergen controls: the written preventive controls that keep an allergen out of a food it does not belong in, and that get the allergens present onto the label.
- 21 CFR 101.4
- Ingredient declaration: every ingredient listed by its common name, in descending order of predominance, on the label of a packaged food.
- 21 CFR 117 subpart G
- Supply-chain programme: the approval and verification a receiving facility runs on a supplier when the hazard is controlled before the ingredient arrives.
The allergens named in this record: milk, peanuts.
Filed under nuts and seeds, sauces, dips and condiments, spices and seasonings and grains, flour and pasta. A product can sit in more than one.
Every product in this recall
The FDA opened 2 enforcement records for this one recall, one per product code. This page carries all of them; the 1 below each have their own page with that product’s lot codes and distribution, and search engines are pointed here for the recall as a whole.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2025-05-21 | Dixit Foods, Sabudana Khichadi, Net Wt. 200 g, Ingredients: Sago (Sabudana), Crushed Groundnuts, Sugar, DesiGhee, Salt, Green Chilli, Cumin Seeds. Allergen Information: May contain Peanuts, Treenuts, Wheat, Sesame, Mustard | Bondsforever, Inc dba Shastha Foods | Undeclared allergens (milk and/or peanuts). | Class II |
Other nuts and seeds recalls for the same reason
These are the closest records in the corpus: the same kind of food, recalled for a hazard this record also names. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
Other records from Bondsforever, Inc dba Shastha Foods
The FDA opens one enforcement record per product code, so several of these are frequently one recall event.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2025-05-21 | Dixit Foods, Sabudana Khichadi, Net Wt. 200 g, Ingredients: Sago (Sabudana), Crushed Groundnuts, Sugar, DesiGhee, Salt, Green Chilli, Cumin Seeds. Allergen Information: May contain Peanuts, Treenuts, Wheat, Sesame, Mustard | Bondsforever, Inc dba Shastha Foods | Undeclared allergens (milk and/or peanuts). | Class II |
All 2025 recalls · All FDA food recall data
21 CFR 117.135(c)(2) is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.