Lower riskFood recall · FDA · Published August 18, 2021
Albanese Mini Gummi Butterflies Recall: Drowsiness Risk from Mixed Supplement
Albanese recalls 7.5oz Mini Gummi Butterflies with Olly Sleep supplement that may cause drowsiness. Consumers should check UPC 634418523525 for affected items.
“Albanese Mini Gummi Butterflies Recall: Drowsiness Risk from Mixed Supplement.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14190-albanese-mini-gummi-butterflies-recall-drowsiness-risk-from-mixed-supplement. Based on FDA recall #F-0984-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0984-2021%22&limit=1).
The FDA announced on Aug. 18, 2021, that Albanese Confectionery Group, Inc. is recalling Albanese World's Best Mini Gummi Butterflies due to the presence of an undeclared Olly Sleep dietary supplement. The agency said the comingled supplement may cause drowsiness.
How to tell if you have it
Brand: Albanese
Product: Albanese World's Best Mini Gummi Butterflies 7.5oz
UPC: 634418523525
Lot code: 1202011130
The hazard
The product contains comingled Olly Sleep dietary supplement which may cause drowsiness, according to the FDA.
Context
GovInfoNow's records show Albanese Confectionery Group, Inc. has two other recalls on record since March 9, 2022, including a May 26, 2022, recall for Rich s Milk Chocolate Peanut Butter Cups due to Salmonella risk and a March 9, 2022, recall for Albanese Dark Chocolate Espresso Bean due to undeclared peanut allergen. Other recent recalls of similar products include Dkiru Magnesium Gummies (May 12, 2026), SB FOOD Yoyo Gummy Tropical (Nov. 21, 2025), and Paw Patrol Heart-Shaped Gummies (Dec. 3, 2025).
How to tell if you have this one
Check for the UPC 634418523525 on the product label. The affected items were produced with Lot number 1202011130.
Brand
Albanese
Product
Albanese World's Best Mini Gummi Butterflies 7.5oz UPC 634418523525
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the UPC 634418523525 and Lot number 1202011130 on the packaging.
Where it went and when
Where it was distributed
Distributed in Michigan and Oklahoma.
Listed by the agency
Not listed
FDA distribution: “Distributors in OK and MI for further distribution to retail stores” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Michigan, Oklahoma.
Recall timeline
FDA terminated this recall 6 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
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-0984-2021 (August 18, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0984-2021 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.