CLASS II Food recall · Reported 13 Feb 2019 · FDA Enforcement Report

SleepWorks Liquid Vitamin & Mineral Herbal Supplement recalled

AdvoCare International is recalling SleepWorks Liquid Vitamin & Mineral Herbal Supplement serving bottles - Net. The recall was initiated on 12 Nov 2018 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLots 1711010, 1711018, 1801168, 1801180, 1802108, 1802123, 1802136, 1803198, 1806019, 1806141, 1806159, 1807068, 1808061, 1809089
Quantity recalled53,205 cartons

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-0843-2019
FDA event ID
81764
Recalling firm
AdvoCare International, Plano, TX
Classification
Class II
Status
Terminated
Recall initiated
12 Nov 2018
FDA classified
7 Feb 2019
Reported
13 Feb 2019
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Other Reasons
Product category
Herbal Supplements

Timeline

12 Nov 2018Recall initiated by company
7 Feb 2019Classified by FDA+87 days
13 Feb 2019Published 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 contains beta phenyl gamma aminobutyric acid HCl.

Product as listed by the FDA

SleepWorks Liquid Vitamin & Mineral Herbal Supplement 12 single serving bottles - 2 Fl Oz (60 mL) Net 24 Fl Oz (720 mL), product code W3721

Where it was distributed

United States

Questions about this recall

Why was it recalled?

Product contains beta phenyl gamma aminobutyric acid HCl.

Which lots are affected?

Lots 1711010, 1711018, 1801168, 1801180, 1802108, 1802123, 1802136, 1803198, 1806019, 1806141, 1806159, 1807068, 1808061, 1809089

Where was it sold?

United States

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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