Luckyberry Cold-Pressed Juice recall

Recalled by Luckyberry · Lawrence, KS, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations

These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.

What was recalled

Luckyberry Cold-Pressed Juice, Mai Tai, Orange Pineapple, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS

Quantity: At least 1 bottle.

Food: Fresh fruit Juice & beverages

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

unknown

Where it was sold

Kansas

FDA's distribution note: To retailers in Lawrence, KS.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm: Luckyberry
Initiated by: Voluntary: Firm initiated
Recall initiated: Oct 30, 2018
In FDA report of: Dec 26, 2018
Terminated: Feb 1, 2019
FDA recall number: F-0774-2019 · event 81492
Official record: FDA enforcement report search

Also recalled with it (8 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class II · Moderate risk Terminated Processing Oct 30, 2018