Monster Energy Company Recall: Product was distributed without going through the retort step.
United States
TerminatedClass II
- Company
- Monster Energy Company
- Product
- Java Monster Loco Moca Coffee & Energy, Net Wt. 15 fl. oz.…
- Recall date
- August 17, 2017
- Terminated
- March 6, 2018
- Source
- FDA
Reason for recall
Product was distributed without going through the retort step.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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 . | Not published in this source record | 7,965 cases | Batch 0365, Lot F1728BF 0 |
Distribution
- To distributors in KS
- MS
- HI
- NC
- AL
- GA
- IA and NJ.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-3545-2017
- Event ID
- 77999
- Status
- Terminated
- Classification
- Class II
- Company
- Monster Energy Company
- Product description
- 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
- Reason
- Product was distributed without going through the retort step.
- Recall initiation date
- August 17, 2017
- Report date
- September 20, 2017
- Classification date
- Not published in this source record
- Termination date
- March 6, 2018
- Distribution pattern
- To distributors in KS, MS, HI, NC, AL, GA, IA and NJ.
- UPC, lot, and code information
- Batch 0365, Lot F1728BF 0
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Monster Energy Company
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Kansas | 1 |
| Mississippi | 1 |
| Hawaii | 1 |
| North Carolina | 1 |
| Alabama | 1 |
| Georgia | 1 |
| Iowa | 1 |
| New Jersey | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
