FDA recall record

Confidence Inc./Confidence U.S.A FP0191, Confidence, Bone-Lock WITHGENISTEIN AND recall — FDA F-1971-2018

Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol (PEG).

Class IIIclassification
F-1971-2018official record ID
Oct 3, 2018report date

Recall record at a glance

Official recordF-1971-2018
CategoryFood Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmConfidence Inc./Confidence U.S.A. Inc.
Report dateOct 3, 2018
Recall initiation dateSep 4, 2018
Quantity538 bottles
LocationPort Washington, NY, United States

Official product description

FP0191, Confidence, Bone-Lock WITHGENISTEIN AND CHLOROPHYLL, A Dietary Supplement, 60 tablets per bottle, UPC: 8 92483 00145 8

Why the product was recalled

Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol (PEG).

Distribution information

NY, MI, TN, FL, IL, WI, NJ, MD, TX, CA, VA, LA, MS, WA, SC, OH, NV, NE, PA, HI,

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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