Bickel's recalls Butter Flavored Popcorn (UPC 7017306021) due to undeclared milk in labeling. Consumers should check packaging for the UPC code and contact the company for details.
“Bickel's Butter Flavored Popcorn Recall: Undeclared Milk Risk.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/14895-bickel-s-butter-flavored-popcorn-recall-undeclared-milk-risk. Based on FDA recall #F-0288-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0288-2021%22&limit=1).
Bickel's Snack Foods Inc voluntarily recalled Butter Flavored Popcorn Artificially Flavored 8oz. due to undeclared milk, the FDA said on Jan. 22, 2021. Owners should contact the company for a refund.
Distribution: Retail stores in FL, GA, CO, NC, SC, VA, TN, AL and TX
The hazard
The product contains undeclared milk due to mislabeling, posing an allergy risk to consumers. The FDA classified this as a Class II recall.
Context
GovInfoNow's records show Bickel's Snack Foods Inc has had three other recalls since May 4, 2016, including undeclared milk hazards in 2023 and 2016. Other recent recalls of similar products include Loard's Peanut Butter Fudge Ice Cream Recall (April 15, 2026), Loard's Butter Brickle Ice Cream Recall (April 15, 2026) and Karison ALSI PINNI 12oz Recall (Jan. 6, 2026).
How to tell if you have this one
Check for the UPC code 7017306021 on the packaging. The product was sold starting March 29, 2021, and is labeled as 'Butter Flavored Popcorn Artificially Flavored 8oz.'
Look for the UPC code 7017306021 on the product label.
Where it went and when
Where it was distributed
Distributed in 9 states.
Listed by the agency
Not listed
FDA distribution: “The product was sold to distributors in Georgia and North Carolina and was distributed to retail stores in FL, GA, CO, NC, SC, CO, VA, TN, AL and TX” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Colorado, Florida, Georgia, North Carolina, South Carolina, Tennessee, Texas, Virginia.
Recall timeline
FDA terminated this recall 13 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-0288-2021 (January 22, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0288-2021 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 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.