Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported July 26, 2017
GnuPharma Sleep 100% Herbal Supplement 60 Capsules
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
GnuPharma Corp. recalled GnuPharma Sleep 100% Herbal Supplement 60 Capsules - a moderate-severity action.
GnuPharma Sleep 100% Herbal Supplement 60 Capsules was recalled by GnuPharma Corp. in July 26, 2017. Reason: 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli). Check the official notice for the remedy. Verify recall #F-0298-2017 with the FDA Food before acting.
The recall
GnuPharma Corp. issued this moderate-severity FDA Food recall-1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli).
- Moderate
- severity level
- Class II
- classification
- July 26, 2017
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-0298-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-0298-2017) was formally reported on July 26, 2017, with the manufacturer initiating the action on May 8, 2017. It is classified under Moderate severity (Class II), with a current status of Terminated. GnuPharma Corp. is listed as the recalling firm, operating out of Owasso, OK. Federal records list the affected scope as 1 bottle.
The documented reason for this recall is: 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli) Distribution data in the federal record shows the product reached: US. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Dietary Supplements recalls over time
Where this recall sits in its category - 2,002 dietary supplements recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
1 bottle
Related Recalls
6
6 from same agency
Product description
GnuPharma Sleep 100% Herbal Supplement 60 Capsules
Reason for recall
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-0298-2017 |
| Date reported | July 26, 2017 |
| Date initiated | May 8, 2017 |
| Recalling firm | GnuPharma Corp. |
| Firm location | Owasso, OK |
| Affected scope | 1 bottle |
| Distribution | US |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-0298-2017) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
GnuPharma Sleep 100% Herbal Supplement 60 Capsules. Recalled by GnuPharma Corp.. Units affected: 1 bottle.
Why was this product recalled? ▼
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
Which agency issued this recall? ▼
This recall was issued by the FDA Food on July 26, 2017. Severity: Moderate. Recall number: F-0298-2017.
Where was the recalled product distributed? ▼
Distribution: US.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0298-2017) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Compare this recall with Blue Bull Extreme Male Enhancement Supplement, total of 15 … →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported July 26, 2017. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.