Food recall

DREAM POPS recall: 100% Plant-Based Dream Pops Vanilla Sky Bites UPC 854097008254

DREAM POPS, of Los Angeles, CA, recalled 100% Plant-Based Dream Pops Vanilla Sky Bites UPC 854097008254 and 3 other products. The FDA's reason: “Undeclared allergen; milk.” The FDA classified it Class I: it could cause serious harm or death. The company began the recall voluntarily on December 20, 2021, and the FDA first listed it in its Enforcement Report of January 19, 2022. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class I

It could cause serious harm or death

Why

Allergen not on the label

Status

Terminated

Closed February 16, 2022

The recall

Company
DREAM POPS (Los Angeles, CA)
Reason, in FDA's words
“Undeclared allergen; milk”
Where it was sold
US nationwide and Canada nationwide
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
89266

The 4 products recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • F-0384-2022 Class I

    100% Plant-Based Dream Pops Vanilla Sky Bites UPC 854097008254

    Codes: Best By Dates 6/28/22-10/21/22

    Quantity: 26,111 cases total - all varieties

  • F-0385-2022 Class I

    100% Plant-Based Dream Pops Berry Dreams Bites UPC 854097008247

    Codes: Best By Dates 6/28/22-10/21/22

    Quantity: 26,111 cases total - all varieties

  • F-0386-2022 Class I

    100% Plant-Based Dream Pops Birthday Cake Bites UPC 854097008339

    Codes: Best By Dates 6/28/22-10/21/22

    Quantity: 26,111 cases total - all varieties

  • F-0387-2022 Class I

    100% Plant-Based Dream Pops Cookie Dough Bites UPC 854097008322

    Codes: Best By Dates 6/28/22-10/21/22

    Quantity: 26,111 cases total - all varieties

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of January 19, 2022.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.