Exact FDA event identifier

Event 77999

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket: August 17, 2017
Product types: Food
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Monster Energy Company

Dossier provenance

Source snapshots represented here

openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Device root-cause evidence is not applicable to this event. No grouped product has the official product type device; this is not an unavailable-enrichment finding.

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 1

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 .

F-3545-2017

Recall number: F-3545-2017
Initiated: August 17, 2017
Classification: Class II
Status: Terminated
Recalling firm: Monster Energy Company
Quantity: 7,965 cases

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Product was distributed without going through the retort step.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Product was distributed without going through the retort step.

Code information

Batch 0365, Lot F1728BF 0

Distribution pattern

To distributors in KS, MS, HI, NC, AL, GA, IA and NJ.