FDA Recall United States TerminatedTerminated: September 12, 2018Historical recordClass II
AdvoCare International, LP
- Product
- AdvoCare Muscle Strength Dietary Supplement with HMB and Sum…
- Published
- May 2, 2018
- Distribution
- United States
AdvoCare International, LP Recall: Product contains beta phenyl gamma aminobutyric acid HCl.
United States
TerminatedClass II
- Company
- AdvoCare International, LP
- Product
- SleepWorks Liquid Vitamin & Mineral Herbal Supplement 12 sin…
- Recall date
- November 12, 2018
- Terminated
- April 17, 2019
- Source
- FDA
Reason for recall
Product contains beta phenyl gamma aminobutyric acid HCl.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| SleepWorks Liquid Vitamin & Mineral Herbal Supplement 12 single serving bottles - 2 Fl Oz (60 mL) Net 24 Fl Oz (720 mL), product code W3721 | Not published in this source record | 53,205 cartons | Lots 1711010, 1711018, 1801168, 1801180, 1802108, 1802123, 1802136, 1803198, 1806019, 1806141, 1806159, 1807068, 1808061, 1809089 |
Distribution
- United States
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0843-2019
- Event ID
- 81764
- Status
- Terminated
- Classification
- Class II
- Company
- AdvoCare International, LP
- Product description
- SleepWorks Liquid Vitamin & Mineral Herbal Supplement 12 single serving bottles - 2 Fl Oz (60 mL) Net 24 Fl Oz (720 mL), product code W3721
- Quantity
- 53,205 cartons
- Reason
- Product contains beta phenyl gamma aminobutyric acid HCl.
- Recall initiation date
- November 12, 2018
- Report date
- February 13, 2019
- Classification date
- Not published in this source record
- Termination date
- April 17, 2019
- Distribution pattern
- United States
- UPC, lot, and code information
- Lots 1711010, 1711018, 1801168, 1801180, 1802108, 1802123, 1802136, 1803198, 1806019, 1806141, 1806159, 1807068, 1808061, 1809089
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: AdvoCare International, LP
Other recalls from AdvoCare International, LP
FDA Recall United States TerminatedTerminated: September 12, 2018Historical recordClass II
AdvoCare International, LP
- Product
- AdvoCare Nighttime Recovery Amino Acid and Herbal Dietary Su…
- Published
- May 2, 2018
- Distribution
- United States
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
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?
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