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Lower risk Food recall · FDA · Published September 8, 2017

Bravo Produce Maradol Papaya Recall: Salmonella Contamination Risk

Bravo Produce is recalling Maradol Papaya due to Salmonella contamination. Products sold in 14kg cardboard boxes may cause foodborne illness. Consumers should avoid eating these items.

🇺🇸 FDA recall #F-3560-2017FoodBravo Produce ›
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Recalling firmBravo Produce Inc524 E San Ysidro Blvd Ste H1 · San Ysidro, CA 92173-3194
✎ GovInfoNow plain-language explainer

What happened, in plain English

Bravo Produce is recalling Maradol Papaya from specific lots due to Salmonella contamination. This poses a risk of foodborne illness if consumed. Read more at govinfonow.com/recall/20438-bravo-produce-maradol-papaya-recall-salmonella-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/20438-bravo-produce-maradol-papaya-recall-salmonella-contamination-risk · Updated October 7, 2026 · FDA enforcement record: FDA #F-3560-2017

Cite this page

“Bravo Produce Maradol Papaya Recall: Salmonella Contamination Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20438-bravo-produce-maradol-papaya-recall-salmonella-contamination-risk. Based on FDA recall #F-3560-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-3560-2017%22&limit=1).

Why it’s dangerous

Salmonella bacteria can cause food poisoning, leading to symptoms like diarrhea, fever, and stomach cramps. The contamination occurred during the growing or processing of the papayas.

Who’s affected

Anyone who purchased Maradol Papaya from Bravo Produce in 14kg cardboard boxes. People who have eaten the recalled papayas are at risk of foodborne illness.

How to tell if you have this one

Check for product codes: 1222335215, 1222635220, 1222335216, and other listed numbers on the box. Products were sold in 14kg cardboard boxes.

  • Brand
    Bravo Produce
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Codes

    Look for specific code numbers on the box: 1222335215, 1222635220, 1222335216, and others listed in the recall.

Where it went and when

Where it was distributed

Distributed in California.

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: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: 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: “Initial distribution in CA only.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California.

Recall timeline

FDA terminated this recall 2 months after the firm started it.

1. Firm started the recall: Sep 8, 201712. FDA classified it Class I: Sep 19, 201723. Published in FDA’s Enforcement Report: Sep 27, 201734. FDA terminated the recall: Nov 21, 201742017
  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-3560-2017 (September 8, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-3560-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 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