Joseph Shalhoub & Son recalls Fruit Punch Fruit Roll due to undeclared wheat
Joseph Shalhoub & Son recalls Fruit Punch Fruit Roll (1 oz) with undeclared wheat. Consumers should check UPC 051063500099 for affected products.
Lower-risk recall
Product contains undeclared wheat.
Contact the company
What happened, in plain English
Joseph Shalhoub & Son is recalling Fruit Punch Fruit Rolls (1 oz) because they contain undeclared wheat. This poses a risk for people with wheat allergies who may experience allergic reactions. Read more at govinfonow.com/recall/21121-joseph-shalhoub-son-recalls-fruit-punch-fruit-roll-due-to.
Source Summary by GovInfoNow · govinfonow.com/recall/21121-joseph-shalhoub-son-recalls-fruit-punch-fruit-roll-due-to · Updated October 8, 2026 · FDA enforcement record: FDA #F-2374-2017
Cite this page
“Joseph Shalhoub & Son recalls Fruit Punch Fruit Roll due to undeclared wheat.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21121-joseph-shalhoub-son-recalls-fruit-punch-fruit-roll-due-to. Based on FDA recall #F-2374-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2374-2017%22&limit=1).
Why it’s dangerous
The product contains wheat that was not listed on the label. This can cause allergic reactions in individuals with wheat allergies. The recall is for all lots of this specific product.
Who’s affected
People with wheat allergies are at risk of allergic reactions from this product. Consumers who purchased the Fruit Punch Fruit Roll (1 oz) with UPC 051063500099 should check if they have the recalled item.
How to tell if you have this one
Check for the Fruit Punch flavor, 1 oz (28g) size, and UPC 051063500099 on the product label.
- Brand
Joseph Shalhoub & Son- Product
joray fruit roll FRUIT PUNCH flavor NET WT 1 OZ. (28g). UPC# 0 51063 50009 9- Category
Food
What to do — step by step
Check Product Label
Look for the UPC code 051063500099 on the Fruit Punch Fruit Roll packaging.
Where it went and when
Where it was distributed
Distributed in Florida and New York.
FDA distribution: “NY and FL” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Florida, New York.
Recall timeline
FDA terminated this recall 11 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- 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-2374-2017 (June 7, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2374-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 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.