The Recall Desk
Agency classClass IOur severity:SevereFDA (Food)·F-0387-2022·Announced 2022-01-19

Dream Pops Cookie Dough Bites Recalled for Undeclared Milk Allergen

Dream Pops 100% Plant-Based Cookie Dough Bites are being recalled because they contain undeclared milk allergen. The product was distributed nationwide in the US and Canada.

The agency’s classification

FDA (Food): Class I

Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 4/5 (Severe).

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The agency classified this recall as Class I — a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death. On that classification alone this is scored Severe; a score of Critical is reserved for recalls where a death or serious injury was reported. The agency gives the reason as: "Undeclared allergen; milk"

Plain-English summary

Dream Pops is recalling 100% Plant-Based Dream Pops Cookie Dough Bites (UPC 854097008322) due to the presence of undeclared milk allergen in the product.

The affected product has Best By Dates ranging from 6/28/22 to 10/21/22. A total of 26,111 cases were distributed nationwide in both the United States and Canada.

Consumers who have purchased this product and have a milk allergy or sensitivity should not consume it. Affected consumers should discontinue use and contact Dream Pops or their retailer for further instructions.

The recalled product

Product
100% Plant-Based Dream Pops Cookie Dough Bites UPC 854097008322
Manufacturer
DREAM POPS
Affected units
26,111

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Best By Dates 6/28/22-10/21/22

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 4 recalled by DREAM POPS under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 4 products in this recall →

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