CLASS II Food recall · Reported 26 Jul 2017 · FDA Enforcement Report

Sleep 100% Herbal Supplement recalled by GnuPharma

GnuPharma is recalling GnuPharma Sleep 100% Herbal Supplement. The recall was initiated on 8 May 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesproducts manufactured prior to May 8th, 2017.
Quantity recalled1 bottle

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-0298-2017
FDA event ID
77506
Recalling firm
GnuPharma, Owasso, OK
Classification
Class II
Status
Terminated
Recall initiated
8 May 2017
FDA classified
18 Jul 2017
Reported
26 Jul 2017
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
E. coli
Product category
Herbal Supplements

Timeline

8 May 2017Recall initiated by company
18 Jul 2017Classified by FDA+71 days
26 Jul 2017Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)

Some strains of E. coli, such as O157:H7, produce a toxin that can cause severe stomach cramps, bloody diarrhea and, in a small number of cases, kidney failure.

Product as listed by the FDA

GnuPharma Sleep 100% Herbal Supplement 60 Capsules

Where it was distributed

US

Questions about this recall

Is Sleep 100% Herbal Supplement recalled?

Yes. GnuPharma recalled Sleep 100% Herbal Supplement on 8 May 2017. The recall is Class II and its status is Terminated. Recall number F-0298-2017.

Why was it recalled?

1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)

Which lots are affected?

products manufactured prior to May 8th, 2017.

Where was it sold?

US

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 21 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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