Recall events
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Event 77506
Event summary
Timeline bucket May 08, 2017
Product types Food
Classifications Class II
Statuses Terminated
Recalling firm wording GnuPharma Corp.
Dossier provenance
Source snapshots represented here
openFDA Food Enforcement
Report-date coverage
June 20, 2012–July 08, 2026
Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.
How coverage and grouping work
Device root-cause evidence is not applicable to this event.
No grouped product has the official product type device; this is not an unavailable-enrichment finding.
Complete imported group
Every recalled product in this event
6 official enforcement rows
Product dates, classifications, firms, and source wording remain attached to their individual rows.
Opening this dossier never hides products that did not match a prior timeline filter.
food · product 1 of 6
GnuPharma Fit 100% Herbal Supplement 60 Capsules
F-0296-2017
Recall number F-0296-2017
Initiated May 08, 2017
Classification Class II
Status Terminated
Quantity 56 bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
Code information products manufactured prior to May 8th, 2017.
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[19526]
FDA event record
· Exact recall-number query on openFDA
food · product 2 of 6
GnuPharma Relief 100% Herbal Supplement 60 Capsules
F-0297-2017
Recall number F-0297-2017
Initiated May 08, 2017
Classification Class II
Status Terminated
Quantity 244 bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
Code information products manufactured prior to May 8th, 2017.
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[20043]
FDA event record
· Exact recall-number query on openFDA
food · product 3 of 6
GnuPharma Sleep 100% Herbal Supplement 60 Capsules
F-0298-2017
Recall number F-0298-2017
Initiated May 08, 2017
Classification Class II
Status Terminated
Quantity 1 bottle
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
Code information products manufactured prior to May 8th, 2017.
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[17993]
FDA event record
· Exact recall-number query on openFDA
food · product 4 of 6
GnuPharma Stress 100% Herbal Supplement 60 Capsules
F-0299-2017
Recall number F-0299-2017
Initiated May 08, 2017
Classification Class II
Status Terminated
Quantity 131 bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
Code information products manufactured prior to May 8th, 2017.
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[18601]
FDA event record
· Exact recall-number query on openFDA
food · product 5 of 6
GnuPharma Foundation 100% Herbal Supplement 60 Capsules
F-0300-2017
Recall number F-0300-2017
Initiated May 08, 2017
Classification Class II
Status Terminated
Quantity 9 bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
Code information products manufactured prior to May 8th, 2017.
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[18086]
FDA event record
· Exact recall-number query on openFDA
food · product 6 of 6
GnuPharma ECS Herbal Tea Relief SAMPLE ONLY
F-0301-2017
Recall number F-0301-2017
Initiated May 08, 2017
Classification Class II
Status Terminated
Quantity 1 unit (4 tablespoons)
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
Code information products manufactured prior to May 8th, 2017.
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[14328]
FDA event record
· Exact recall-number query on openFDA
