Lower riskFood recall · FDA · Published September 30, 2021
Best Foods Sundelight Golden Raisins Recall: Undeclared Sulfites Hazard
Best Foods recalls Sundelight Golden Raisins (7oz pouches) due to undeclared sulfites. Consumers should check UPC 14760 84059 and lot #244083120 for affected products.
“Best Foods Sundelight Golden Raisins Recall: Undeclared Sulfites Hazard.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14094-best-foods-sundelight-golden-raisins-recall-undeclared-sulfites-hazard. Based on FDA recall #F-0121-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0121-2022%22&limit=1).
Best Foods NJ, Inc. recalled Sundelight Golden Raisins due to undeclared sulfites, the FDA said on Sept. 30, 2021. Consumers should discard the product or contact the company for a refund.
How to tell if you have it
Sundelight Golden Raisins Net Wt 7oz
UPC: 14760 84059
Lot # 244083120
The hazard
The product contains undeclared sulfites, which can cause allergic reactions in sensitive individuals. The recall is classified as Class I.
Context
GovInfoNow's records show Best Foods NJ, Inc. has had three other recalls since March 27, 2015, including a March 27, 2015, recall of Deer Brand Golden Raisin for undeclared sulfites. Other recent recalls of similar products include Elegant Foods Golden Raisins Recall (July 24, 2026), Elegant Foods Coconut Flakes Recall (July 24, 2026), and Sofit Seedless Red Dates Recall (Nov. 4, 2025).
How to tell if you have this one
Check for Sundelight Golden Raisins in 7oz plastic pouches with UPC 14760 84059 and lot number 244083120. The product was sold in cases of 20 pouches.
Brand
Best Foods
Product
Sundelight Golden Raisins Net Wt 7oz. UPC: 14760 84059. Plastic pouches. 20 pouches/per case
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the UPC 14760 84059 and lot number 244083120 on the plastic pouch.
Where it went and when
Where it was distributed
Distributed in 3 states.
Listed by the agency
Not listed
FDA distribution: “Distributed to retail stores in MD, NJ, and NY.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Maryland, New Jersey, New York.
Recall timeline
FDA terminated this recall 20 months after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-0121-2022 (September 30, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0121-2022 to see it in context.
Plain-language summary written by qwen3:4b on October 4, 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.