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Lower risk Food recall · FDA · Published September 4, 2018

Confidence Bone-Lock Dietary Supplement Recall: Undeclared Ingredients

Confidence recalls Bone-Lock dietary supplement with undeclared ingredients like HPMC, Titanium Dioxide, and PEG. Consumers should check product details to determine if affected.

🇺🇸 FDA recall #F-1971-2018FoodConfidence ›
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Contact the company

Recalling firmConfidence Inc./Confidence U.S.A. Inc.138 Haven Ave · Port Washington, NY 11050-3924
✎ GovInfoNow plain-language explainer

What happened, in plain English

Confidence is recalling Bone-Lock dietary supplements that contain undeclared ingredients. This could pose risks for people with allergies or sensitivities to these ingredients. Read more at govinfonow.com/recall/18697-confidence-bone-lock-dietary-supplement-recall-undeclared-ingredients.

Source Summary by GovInfoNow · govinfonow.com/recall/18697-confidence-bone-lock-dietary-supplement-recall-undeclared-ingredients · Updated October 6, 2026 · FDA enforcement record: FDA #F-1971-2018

Cite this page

“Confidence Bone-Lock Dietary Supplement Recall: Undeclared Ingredients.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/18697-confidence-bone-lock-dietary-supplement-recall-undeclared-ingredients. Based on FDA recall #F-1971-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1971-2018%22&limit=1).

Why it’s dangerous

The supplement contains undeclared ingredients that some people may be allergic to or sensitive to. These ingredients include Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, and Polyethylene Glycol (PEG).

Who’s affected

People who own or use Confidence Bone-Lock supplements with the specific UPC 8 92483 and lot number 090616 are affected. Those with allergies to HPMC, Titanium Dioxide, or PEG are at higher risk.

How to tell if you have this one

Check for the product name 'Bone-Lock WITHGENISTEIN AND CHLOROPHYLL', 60 tablets per bottle, UPC 8 92483, and lot number 090616.

  • Brand
    Confidence
  • Product
    FP0191, Confidence, Bone-Lock WITHGENISTEIN AND CHLOROPHYLL, A Dietary Supplement, 60 tablets per bottle, UPC: 8 92483
  • Category
    Food
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Status
    Terminated
  • Distribution
    NY, MI, TN, FL, IL, WI, NJ, MD, TX, CA, VA, LA, MS, WA, SC, OH, NV, NE, PA, HI,
Recall numberProduct, codes & lotsQuantityClass
F-1971-2018FP0191, Confidence, Bone-Lock WITHGENISTEIN AND CHLOROPHYLL, A Dietary Supplement, 60 tablets per bottle, UPC: 8 92483 00145 8; Lot# 090616538 bottlesClass III
F-1972-2018FP0392, For-Men-10, All Natural Formula to Overall Men's Health, A Dietary Supplement, 60 Tablets, UPC: 8 92483 00139 7; Lot# 0201162016 bottlesClass II
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the UPC 8 92483 and lot number 090616 on the supplement label.

Where it went and when

Where it was distributed

Distributed in 20 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: yesNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: not listedCONebraska: yesNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: yesVAMaryland: yesMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: yesTNNorth Carolina: not listedNCSouth Carolina: yesSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: yesLAMississippi: yesMSAlabama: not listedALGeorgia: not listedGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “NY, MI, TN, FL, IL, WI, NJ, MD, TX, CA, VA, LA, MS, WA, SC, OH, NV, NE, PA, HI,” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, Florida, Hawaii, Illinois, Louisiana, Maryland, Michigan, Mississippi, Nebraska, Nevada, New Jersey, New York, Ohio, Pennsylvania, South Carolina, Tennessee, Texas, Virginia, Washington, Wisconsin.

Recall timeline

FDA terminated this recall 14 months after the firm started it.

1. Firm started the recall: Sep 4, 201812. FDA classified it Class III: Sep 21, 201823. Published in FDA’s Enforcement Report: Oct 3, 201834. FDA terminated the recall: Nov 5, 2019420182019
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-1971-2018 (September 4, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1971-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 6, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA