Confidence Glucosamine Plus Recalled for Undeclared Ingredients
Confidence Inc. is recalling Glucosamine Plus tablets because they contain undeclared ingredients, including Hydroxypropyl Methylcellulose and Titanium Dioxide.
What this means for you
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The FDA classified this recall as Class III, which by definition indicates the product is unlikely to cause adverse health consequences, aligning with the 'Low' severity criteria for minor labeling or documentation issues.
Plain-English summary
Confidence Inc./Confidence U.S.A. Inc. is recalling FP0392, Confidence, Glucosamine Plus, with White Willow Bark & Boswella, 90 Extended Release Tablets. The product is being recalled because it contains undeclared ingredients, specifically Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol 400 and 800 (PEG), and Triacetin.
The recall affects 5,650 bottles distributed nationwide. The affected lot numbers are 010216, 070816, 090117, and 100817. The product can be identified by the UPC number 8 10891 02253 7.
Consumers should stop using the product and return it to the place of purchase for a refund. This recall is classified as Class III by the FDA, indicating that the product is unlikely to cause adverse health consequences.
The recalled product
- Product
- FP0392, Confidence, Glucosamine Plus, with White Willow Bark & Boswella, 90 Extended Release Tablets, UPC# 8 10891 02253 7
- Manufacturer
- Confidence Inc./Confidence U.S.A. Inc.
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 5,650
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot# 010216 Lot# 070816 Lot# 090117 Lot# 100817
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 4 recalled by Confidence Inc./Confidence U.S.A. Inc. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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