Recall events
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Event 80995
Event summary
Timeline bucket September 04, 2018
Product types Food
Classifications Class II and Class III
Statuses Terminated
Recalling firm wording Confidence Inc./Confidence U.S.A. Inc.
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
2 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 2
FP0191, Confidence, Bone-Lock WITHGENISTEIN AND CHLOROPHYLL, A Dietary Supplement, 60 tablets per bottle, UPC: 8 92483 00145 8
F-1971-2018
Recall number F-1971-2018
Initiated September 04, 2018
Classification Class III
Status Terminated
Quantity 538 bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol (PEG).
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol (PEG).
Code information Lot# 090616
Distribution pattern NY, MI, TN, FL, IL, WI, NJ, MD, TX, CA, VA, LA, MS, WA, SC, OH, NV, NE, PA, HI,
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[4036]
FDA event record
· Exact recall-number query on openFDA
food · product 2 of 2
FP0392, For-Men-10, All Natural Formula to Overall Men's Health, A Dietary Supplement, 60 Tablets, UPC: 8 92483 00139 7
F-1972-2018
Recall number F-1972-2018
Initiated September 04, 2018
Classification Class II
Status Terminated
Quantity 2016 bottles
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol (PEG), Triacetin, FD&C Yellow #6 (Sunset Yellow FCF), FD&C Red #40 (Allura Red AC), FD&C Blue #1 (Aluminum Lake).
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol (PEG), Triacetin, FD&C Yellow #6 (Sunset Yellow FCF), FD&C Red #40 (Allura Red AC), FD&C Blue #1 (Aluminum Lake).
Code information Lot# 020116
Distribution pattern NY, MI, TN, FL, IL, WI, NJ, MD, TX, CA, VA, LA, MS, WA, SC, OH, NV, NE, PA, HI,
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[2937]
FDA event record
· Exact recall-number query on openFDA