DREAM POPS recalls 100% Plant-Based Vanilla Sky Bites due to undeclared milk allergen. Products sold between 6/28/22 and 10/21/22 with UPC 854097008254 may contain milk.
📍Recalling firmDREAM POPS1880 Century Park E Ste 200 · Los Angeles, CA 90067-1602
✎ GovInfoNow plain-language explainer
DREAM POPS is recalling 100% Plant-Based Vanilla Sky Bites because they contain undeclared milk, which poses a risk for people with milk allergies. This recall affects products sold between June 28, 2022, and October 21, 2022, with UPC 854097008254. Read more at govinfonow.com/recall/13547-dream-pops-vanilla-sky-bites-recall-undeclared-milk-allergen.
“DREAM POPS Vanilla Sky Bites Recall: Undeclared Milk Allergen.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/13547-dream-pops-vanilla-sky-bites-recall-undeclared-milk-allergen. Based on FDA recall #F-0384-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0384-2022%22&limit=1).
The FDA announced on Dec. 20, 2021, that Dream Pops voluntarily recalled 100% Plant-Based Dream Pops Vanilla Sky Bites due to undeclared milk allergens. The recall affects 26,111 cases distributed nationwide in the U.S. and Canada.
The product contains undeclared milk, which poses a risk to individuals with milk allergies. The FDA classified this as a Class I recall.
Context
GovInfoNow's records show Dream Pops has been involved in previous recalls, including the D'Dioses Vanilla Ice Pop Recall on May 4, 2026, for potentially containing undeclared allergens. Other recent recalls of similar products include the D'Dioses Rompope Ice Pops Recall (May 4, 2026) and the D'Dioses Tamarindo Ice Pop Recall (May 4, 2026), both citing undeclared allergens.
How to tell if you have this one
Check for the UPC 854097008254 on the product label. Products were sold between June 28, 2022, and October 21, 2022.
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class I
Status
Terminated
Distribution
US nationwide and Canada nationwide
Recall number
Product, codes & lots
F-0384-2022
100% Plant-Based Dream Pops Vanilla Sky Bites UPC 854097008254; Best By Dates 6/28/22-10/21/22
F-0385-2022
100% Plant-Based Dream Pops Berry Dreams Bites UPC 854097008247; Best By Dates 6/28/22-10/21/22
F-0386-2022
100% Plant-Based Dream Pops Birthday Cake Bites UPC 854097008339; Best By Dates 6/28/22-10/21/22
F-0387-2022
100% Plant-Based Dream Pops Cookie Dough Bites UPC 854097008322; Best By Dates 6/28/22-10/21/22
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the UPC 854097008254 on the package to identify recalled items.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “US nationwide and Canada nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA terminated this recall 58 days 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-0384-2022 (December 20, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0384-2022 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.