CLASS II Food recall · Reported 20 Sep 2017 · FDA Enforcement Report
Java Monster Loco Moca Coffee & Energy recalled by Monster Energy
Monster Energy is recalling Java Monster Loco Moca Coffee & Energy, distributed in 8 states. The recall was initiated on 17 Aug 2017 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-3545-2017
- FDA event ID
- 77999
- Recalling firm
- Monster Energy, Corona, CA
- Brand
- Java Monster
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 17 Aug 2017
- FDA classified
- 14 Sep 2017
- Reported
- 20 Sep 2017
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Other Reasons
- Product category
- Herbal Supplements
Timeline
| 17 Aug 2017 | Recall initiated by company | |
| 14 Sep 2017 | Classified by FDA | +28 days |
| 20 Sep 2017 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product was distributed without going through the retort step.
Product as listed by the FDA
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 .
Where it was distributed
To distributors in KS, MS, HI, NC, AL, GA, IA and NJ.
AlabamaGeorgiaHawaiiIowaKansasMississippiNorth CarolinaNew Jersey
Questions about this recall
Why was it recalled?
Product was distributed without going through the retort step.
Which lots are affected?
Batch 0365, Lot F1728BF 0
Where was it sold?
To distributors in KS, MS, HI, NC, AL, GA, IA and NJ.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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