Luckyberry Recalls Unpasteurized Cold-Pressed Juice for Regulatory Violation
Luckyberry is recalling unpasteurized cold-pressed juice products because they were manufactured and distributed in violation of FDA regulations.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the source text does not report any illnesses or injuries, fitting the criteria for a moderate severity recall involving regulatory violations without confirmed harm.
Plain-English summary
Luckyberry is recalling at least four bottles of Luckyberry Cold-Pressed Juice, Reset, Carrot, Apple, Ginger, Lemon, 16 FL OZ. The product was manufactured at Luckyberry Juice Cafe in Lawrence, KS, and distributed to retailers in Lawrence, KS.
The recall was initiated because the firm manufactured and distributed unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations. The source text does not report any specific illnesses or injuries associated with the product.
Consumers who purchased this product should stop using it and contact the recalling firm for further instructions.
The recalled product
- Product
- Luckyberry Cold-Pressed Juice, Reset, Carrot, Apple, Ginger, Lemon, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
- Manufacturer
- Luckyberry
- Category
- Food — Juice
- Affected units
- 4
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)
- unknown
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 9 recalled by Luckyberry 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.
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