Food recall
Confidence Inc./Confidence U.S.A. Inc. recall: FP0191, Confidence, Bone-Lock WITHGENISTEIN AND CHLOROPHYLL, A Dietary Supplement
Confidence Inc./Confidence U.S.A. Inc., of Port Washington, NY, recalled FP0191, Confidence, Bone-Lock WITHGENISTEIN AND CHLOROPHYLL, A Dietary Supplement and 1 other product. The FDA's reason: “Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol (PEG).” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on September 4, 2018, and the FDA first listed it in its Enforcement Report of October 3, 2018. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.
How serious
Class II
It could cause temporary or minor harm
Why
Other ingredient not on the label (sulfites, dyes...)
Status
Terminated
Closed November 5, 2019
The recall
- Company
- Confidence Inc./Confidence U.S.A. Inc. (Port Washington, NY)
- Reason, in FDA's words
- “Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol (PEG).”
- Where it was sold
- NY, MI, TN, FL, IL, WI, NJ, MD, TX, CA, VA, LA, MS, WA, SC, OH, NV, NE, PA, HI,
- Recall began
- , by the company
- FDA classified it
- First in an FDA Enforcement Report
- FDA event number
- 80995
The 2 products recalled
As the FDA describes them, with the codes that tell whether a package is part of the recall.
-
F-1971-2018 Class III
FP0191, Confidence, Bone-Lock WITHGENISTEIN AND CHLOROPHYLL, A Dietary Supplement, 60 tablets per bottle, UPC: 8 92483 00145 8
Codes: Lot# 090616
Quantity: 538 bottles
-
F-1972-2018 Class II
FP0392, For-Men-10, All Natural Formula to Overall Men's Health, A Dietary Supplement, 60 Tablets, UPC: 8 92483 00139 7
Codes: Lot# 020116
Quantity: 2016 bottles
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Source and notes
U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of October 3, 2018.
Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.