Food Recall Check
Class II · Moderate risk Terminated Initiated Aug 17, 2017 (9 years ago)

Java Monster Loco Moca Coffee & Energy recall

Recalled by Monster Energy Company · Corona, CA, United States

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

Why it was recalled

Product was distributed without going through the retort step.

See the recall's own reason text for the specifics. All other reasons recalls.

What was recalled

Java Monster Loco Moca Coffee & Energy, Net Wt. 15 fl. oz. (443 mL); UPC 0 70847 81271 5; INGREDIENTS: BREWED COFFEE (FILTERED WATER., COFFEE, CONDENSED SKIM MILK. SUGAR, HEAVY CREAM. GLUCOSE. NATURAL FLAVORS. TAURlNE,. SODIUM CITRATE, MICiOCRYSTALLINE CELLULOSE. PANAX GINSENG EXTRACT, ASCORBIC ACID (VIT. C), TRICALCIUM PHOSPHATE, CARRAGEENAN, CAFFEINE, SODIUM ALGINATE. NIACINAMIDE (Vit B3), SUCRALOSE. COLOR ADDED. D-GLUCURONOLACTONE, GUARANA EXTRACT. INOSITOL, L-CARtJITINE L¿TARTRATE. PYRIQDXINE HYDROCHLORIDE (Vit. B6), RIBOFLAVIN (Vit. B1). MALTODEXTRIN. CONTAINS MILK .

Quantity: 7,965 cases

Food: 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.

Batch 0365, Lot F1728BF 0

Where it was sold

Alabama Georgia Hawaii Iowa Kansas Mississippi North Carolina New Jersey

FDA's distribution note: To distributors in KS, MS, HI, NC, AL, GA, IA and NJ.

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
Monster Energy Company
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 17, 2017
In FDA report of
Sep 20, 2017
Terminated
Mar 6, 2018
FDA recall number
F-3545-2017 · event 77999
Official record
FDA enforcement report search

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