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Stop using now Food recall · FDA · Published September 22, 2016

Bikaji Chowpati Bhelpuri Recalled for Salmonella Risk

Krishna Food Corp recalls Bikaji Chowpati Bhelpuri due to Salmonella contamination. Check your batch and expiration dates immediately.

🇺🇸 FDA recall #F-0051-2017FoodBikaji ›
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Recalling firmKRISHNA FOOD CORP59 Ariel Ct · Branchburg, NJ 08853-4233
✎ GovInfoNow plain-language explainer

What happened, in plain English

Krishna Food Corp is recalling Bikaji Chowpati Bhelpuri because FDA testing found Salmonella contamination in the product. This recall affects specific items sold in New Jersey, New York, and Pennsylvania. Consumers should check their pantry for the affected batch numbers and expiration dates. Read more at govinfonow.com/recall/23142-bikaji-chowpati-bhelpuri-recalled-for-salmonella-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/23142-bikaji-chowpati-bhelpuri-recalled-for-salmonella-risk · Updated October 11, 2026 · FDA enforcement record: FDA #F-0051-2017

Cite this page

“Bikaji Chowpati Bhelpuri Recalled for Salmonella Risk.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/23142-bikaji-chowpati-bhelpuri-recalled-for-salmonella-risk. Based on FDA recall #F-0051-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0051-2017%22&limit=1).

Why it’s dangerous

The product contains Salmonella, a bacterium that can cause foodborne illness. Ingesting contaminated food can lead to symptoms such as diarrhea, fever, and abdominal cramps, which can be serious for vulnerable populations.

Who’s affected

Consumers who purchased Bikaji Chowpati Bhelpuri from retail stores or restaurants in New Jersey, New York, and Pennsylvania are likely affected. Individuals who consume this specific lot of food are at risk of Salmonella infection.

How to tell if you have this one

Look for Bikaji Chowpati Bhelpuri with a net weight of 300 g (10.58 oz) and Item No: B022. Check the packaging for Batch No: 2016 F 97 and a Best Before date of June 2017. The product is labeled as Product of India.

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

What to do — step by step

  1. Check your product

    Verify if you have Bikaji Chowpati Bhelpuri with Item No: B022, Batch No: 2016 F 97, and Best Before: June 2017.

  2. Stop consuming the product

    Do not eat the recalled Bhelpuri due to the risk of Salmonella contamination.

Where it went and when

Where it was distributed

Distributed in 3 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: yesPANew 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: “NJ, NY, PA via Retail stores and restaurants” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: New Jersey, New York, Pennsylvania.

Recall timeline

FDA terminated this recall 21 months after the firm started it.

1. Firm started the recall: Sep 22, 201612. FDA classified it Class I: Oct 7, 201623. Published in FDA’s Enforcement Report: Oct 19, 201634. FDA terminated the recall: Jun 19, 2018420162018
  1. Firm started the recall
  2. FDA classified it Class I
  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 #F-0051-2017 (September 22, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0051-2017 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 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