FDA Recall United States Terminated Historical recordClass II
Confidence Inc./Confidence U.S.A. Inc.
- Product
- FP0392, For-Men-10, All Natural Formula to Overall Men's Hea…
- Published
- October 3, 2018
- Distribution
- Multiple states
Confidence Inc./Confidence U.S.A. Inc. Recall: Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol (PEG).
United States
TerminatedClass III
- Company
- Confidence Inc./Confidence U.S.A. Inc.
- Product
- FP0191, Confidence, Bone-Lock WITHGENISTEIN AND CHLOROPHYLL,…
- Recall date
- September 4, 2018
- Terminated
- November 5, 2019
- Source
- FDA
Reason for recall
Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol (PEG).
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| FP0191, Confidence, Bone-Lock WITHGENISTEIN AND CHLOROPHYLL, A Dietary Supplement, 60 tablets per bottle, UPC: 8 92483 00145 8 | Not published in this source record | 538 bottles | Lot# 090616 |
Distribution
- NY
- MI
- TN
- FL
- IL
- WI
- NJ
- MD
- TX
- CA
- VA
- LA
- MS
- WA
- SC
- OH
- NV
- NE
- PA
- HI
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1971-2018
- Event ID
- 80995
- Status
- Terminated
- Classification
- Class III
- Company
- Confidence Inc./Confidence U.S.A. Inc.
- Product description
- FP0191, Confidence, Bone-Lock WITHGENISTEIN AND CHLOROPHYLL, A Dietary Supplement, 60 tablets per bottle, UPC: 8 92483 00145 8
- Quantity
- 538 bottles
- Reason
- Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol (PEG).
- Recall initiation date
- September 4, 2018
- Report date
- October 3, 2018
- Classification date
- Not published in this source record
- Termination date
- November 5, 2019
- Distribution pattern
- NY, MI, TN, FL, IL, WI, NJ, MD, TX, CA, VA, LA, MS, WA, SC, OH, NV, NE, PA, HI,
- UPC, lot, and code information
- Lot# 090616
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Letter
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 80995 with 1 other product entry in Public Health Trace.
Responsible company: Confidence Inc./Confidence U.S.A. Inc.
Other recalls from Confidence Inc./Confidence U.S.A. Inc.
FDA Recall United States Terminated Historical recordClass II
Confidence Inc./Confidence U.S.A. Inc.
- Product
- FP0392, For-Men-10, All Natural Formula to Overall Men's Hea…
- Published
- October 3, 2018
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass III
Confidence Inc./Confidence U.S.A. Inc.
- Product
- FP0391 Confidence, Glucosamine Plus, With Hyaluronic Acid +…
- Published
- August 22, 2018
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Confidence Inc./Confidence U.S.A. Inc.
- Product
- FP0692, Confidence, Prenatal Multi-V + DHA, 90 tablets per b…
- Published
- August 22, 2018
- Distribution
- Nationwide
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| New York | 1 |
| Michigan | 1 |
| Tennessee | 1 |
| Florida | 1 |
| Illinois | 1 |
| Wisconsin | 1 |
| New Jersey | 1 |
| Maryland | 1 |
| Texas | 1 |
| California | 1 |
| Virginia | 1 |
| Louisiana | 1 |
| Mississippi | 1 |
| Washington | 1 |
| South Carolina | 1 |
| Ohio | 1 |
| Nevada | 1 |
| Nebraska | 1 |
| Pennsylvania | 1 |
| Hawaii | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class III mean?
A situation in which use of or exposure to a product is not likely to cause adverse health consequences.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
