Fruits Du Sud Golden Seedless Raisins Recall: Undeclared Sulfites
P. East Trading Corp. recalls Fruits Du Sud Golden Seedless Raisins (30 lb boxes, Lot FDS T499/18, April 2018) due to undeclared sulfites. Consumers should check labels and contact the company for details.
Lower-risk recall
Product contains undeclared sulfites.
Contact the company
What happened, in plain English
P. East Trading Corp. is recalling Fruits Du Sud Golden Seedless Raisins from 30 lb boxes with Lot No. FDS T499/18 produced in April 2018. The raisins contain undeclared sulfites, which can cause allergic reactions in sensitive individuals. Read more at govinfonow.com/recall/18411-fruits-du-sud-golden-seedless-raisins-recall-undeclared-sulfites.
Source Summary by GovInfoNow · govinfonow.com/recall/18411-fruits-du-sud-golden-seedless-raisins-recall-undeclared-sulfites · Updated October 6, 2026 · FDA enforcement record: FDA #F-0348-2019
Cite this page
“Fruits Du Sud Golden Seedless Raisins Recall: Undeclared Sulfites.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/18411-fruits-du-sud-golden-seedless-raisins-recall-undeclared-sulfites. Based on FDA recall #F-0348-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0348-2019%22&limit=1).
Why it’s dangerous
Sulfites are preservatives that can cause allergic reactions in some people. The product contains sulfites without being declared on the label, which is a regulatory violation and a potential health risk for sensitive individuals.
Who’s affected
People who purchased Fruits Du Sud Golden Seedless Raisins in 30 lb boxes with Lot No. FDS T499/18 from April 2018. Those with sulfite allergies are at higher risk.
How to tell if you have this one
Check for 30 lb boxes labeled 'Fruits Du Sud Golden Seedless Raisins' with Lot No. FDS T499/18 and a production date of April 2018. The product is from South Africa.
- Brand
Fruits Du Sud- Category
Food
What to do — step by step
Check Product Label
Look for Lot No. FDS T499/18 and production date of April 2018 on the box.
Where it went and when
Where it was distributed
Distributed in New Jersey and New York.
FDA distribution: “Products were distributed to both retail customers in New York State with one customer in New Jersey.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: New Jersey, New York.
Recall timeline
FDA terminated this recall 2 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-0348-2019 (October 10, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0348-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 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.