Confidence Glucosamine Plus Tablets Recall: Undeclared Ingredients
Confidence recalls Glucosamine Plus tablets with undeclared ingredients like HPMC, Titanium Dioxide, and PEG. Consumers should check product details to determine if affected.
Lower-risk recall
Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol 400 and 800 (PEG), Triacetin
Contact the company
What happened, in plain English
Confidence is recalling a specific glucosamine supplement product due to undeclared ingredients. This could pose risks for people with allergies to these ingredients, though the recall doesn't specify serious injury risks. Read more at govinfonow.com/recall/18805-confidence-glucosamine-plus-tablets-recall-undeclared-ingredients.
Source Summary by GovInfoNow · govinfonow.com/recall/18805-confidence-glucosamine-plus-tablets-recall-undeclared-ingredients · Updated October 6, 2026 · FDA enforcement record: FDA #F-1813-2018
Cite this page
“Confidence Glucosamine Plus Tablets Recall: Undeclared Ingredients.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/18805-confidence-glucosamine-plus-tablets-recall-undeclared-ingredients. Based on FDA recall #F-1813-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1813-2018%22&limit=1).
Why it’s dangerous
The product contains undeclared ingredients that some people may be allergic to. These ingredients include Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, and Polyethylene Glycol 400 and 800 (PEG). Allergic reactions could range from mild to severe.
Who’s affected
People who purchased the Confidence Glucosamine Plus tablets with White Willow Bark & Boswella, 90 Extended Release Tablets (UPC# 8 10891) 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 'Confidence Glucosamine Plus, with White Willow Bark & Boswella, 90 Extended Release Tablets' and UPC# 8 10891. Affected lots include 010216, 070816, 090117, and 100817.
- Brand
Confidence- Product
FP0392, Confidence, Glucosamine Plus, with White Willow Bark & Boswella, 90 Extended Release Tablets, UPC# 8 10891- Category
Food
All 4 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
Nationwide
| Recall number | Product, codes & lots | Class |
|---|---|---|
| F-1813-2018 | FP0392, Confidence, Glucosamine Plus, with White Willow Bark & Boswella, 90 Extended Release Tablets, UPC# 8 10891 02253 7; Lot# 010216 Lot# 070816 Lot# 090117 Lot# 100817 | Class III |
| F-1814-2018 | FP0292 Confidence Nitro-Cross 60s, UPC# 8 92483 00155 7; Lot# 070616 | Class III |
| F-1815-2018 | FP0692, Confidence, Prenatal Multi-V + DHA, 90 tablets per bottle, UPC# 8 10891 02056 4; Lot# 110516 | Class II |
| F-1816-2018 | FP0391 Confidence, Glucosamine Plus, With Hyaluronic Acid + Curcumin & Boswellia, 60 Extended Release Tablets, UPC: 8 92483 00106 9; Lot# 030616 | Class III |
What to do — step by step
Check Product Details
Look for the product name and UPC# 8 10891 on the packaging to confirm if you have the recalled item.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 15 months after the firm started it.
- Firm started the recall
- FDA classified it Class III
- Published in FDA’s Enforcement Report
- 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-1813-2018 (July 26, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1813-2018 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.