Agrosons Papayas Maradol Cavi Recall: Salmonella Contamination Risk
Agrosons LLC recalls Papayas Maradol cavi due to potential Salmonella contamination. Consumers should avoid these products from lots 3044, 3045, and 3050.
Lower-risk recall
Product may be contaminated with Salmonella.
Contact the company
What happened, in plain English
Agrosons LLC is recalling Papayas Maradol cavi that may be contaminated with Salmonella. This poses a risk of foodborne illness, so affected consumers should avoid using these products. Read more at govinfonow.com/recall/20575-agrosons-papayas-maradol-cavi-recall-salmonella-contamination-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/20575-agrosons-papayas-maradol-cavi-recall-salmonella-contamination-risk · Updated October 7, 2026 · FDA enforcement record: FDA #F-3481-2017
Cite this page
“Agrosons Papayas Maradol Cavi Recall: Salmonella Contamination Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20575-agrosons-papayas-maradol-cavi-recall-salmonella-contamination-risk. Based on FDA recall #F-3481-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-3481-2017%22&limit=1).
Why it’s dangerous
Salmonella is a bacteria that can cause food poisoning, leading to symptoms like diarrhea, fever, and abdominal cramps. Contaminated papayas may not show visible signs of spoilage.
Who’s affected
Consumers who purchased Papayas Maradol cavi from Agrosons LLC between the dates of production and distribution. Those with compromised immune systems are at higher risk for foodborne illness.
How to tell if you have this one
Check the lot numbers on the packaging: 3044, 3045, or 3050. These papayas were grown by CARICA DE CAMPECHE and distributed by Agrosons LLC.
- Brand
Agrosons- Category
Food
What to do — step by step
Check Product Lot Number
Look for lot numbers 3044, 3045, or 3050 on the packaging.
Where it went and when
Where it was distributed
Distributed in 3 states.
FDA distribution: “NY, CT, NJ” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Connecticut, New Jersey, New York.
Recall timeline
FDA terminated this recall 14 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- 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-3481-2017 (August 3, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-3481-2017 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.