Why it was recalled
The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations
Product description
Luckyberry Cold-Pressed Juice, Merc Blend, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
Lot numbers, UPCs & expiration codes
unknown
Where it was sold
To retailers in Lawrence, KS.
What to do if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- F-0769-2019
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Oct 30, 2018
- FDA report date
- Dec 26, 2018
- Quantity
- At least 9 bottles
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Luckyberry
Original FDA data
Every field from FDA enforcement report F-0769-2019, exactly as published.
Show all FDA fields
- City
- Lawrence
- State
- KS
- Status
- Terminated
- Country
- United States
- Event ID
- 81492
- Address
- 845 Massachusetts St
- Code information
- unknown
- Postal code
- 66044-2657
- Report date
- Dec 26, 2018
- Product type
- Food
- Recall number
- F-0769-2019
- Classification
- Class II
- Recalling firm
- Luckyberry
- Product quantity
- At least 9 bottles
- Termination date
- Feb 1, 2019
- Reason for recall
- The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Luckyberry Cold-Pressed Juice, Merc Blend, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
- Distribution pattern
- To retailers in Lawrence, KS.
- Recall initiation date
- Oct 30, 2018
- Initial firm notification
- Visit
- Center classification date
- Jan 30, 2019