Food recall: FP0191, Confidence, Bone-Lock WITHGENISTEIN AND CHLOROPHYLL, A Dietary Supplement, 60 tablets per bottle, UPC: 8 92483 0
Confidence Inc./Confidence U.S.A. Inc. (Port Washington, NY) initiated this food recall on 4 Sep 2018; FDA lists 2 product records under event 80995, classified Class II.
FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 56% of the 578 food enforcement events initiated in 2018 carry the same class.
Status: Terminated, terminated 5 Nov 2019. Initiation: voluntary: firm initiated. Confidence Inc./Confidence U.S.A. Inc. has 2 enforcement events on this register, with a median of 4 product records per event.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Confidence Inc./Confidence U.S.A. Inc., Port Washington, NY.
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)."
Distribution
"NY, MI, TN, FL, IL, WI, NJ, MD, TX, CA, VA, LA, MS, WA, SC, OH, NV, NE, PA, HI,"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-1971-2018 | FP0191, Confidence, Bone-Lock WITHGENISTEIN AND CHLOROPHYLL, A Dietary Supplement, 60 tablets per bottle, UPC: 8 92483 00145 8 | 538 bottles | Class III | Terminated | 3 Oct 2018 |
| F-1972-2018 | FP0392, For-Men-10, All Natural Formula to Overall Men's Health, A Dietary Supplement, 60 Tablets, UPC: 8 92483 00139 7 | 2016 bottles | Class II | Terminated | 3 Oct 2018 |
Context
Other enforcement events for Confidence Inc./Confidence U.S.A. Inc.
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 26 Jul 2018 | FP0392, Confidence, Glucosamine Plus, with White Willow Bark & Boswella, 90 Extended Release Tablets, UPC# 8 10891 02253 | Food | Class II | 4 |
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "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)."
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Where was the product distributed?
FDA's distribution pattern field reads: "NY, MI, TN, FL, IL, WI, NJ, MD, TX, CA, VA, LA, MS, WA, SC, OH, NV, NE, PA, HI,"
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 5 Nov 2019. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.