FP0692 — Class II food recall F-1815-2018
Terminated recall by Confidence Inc./Confidence U.S.A. Inc., reported 2018-08-22, distributed nationwide. Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene
| Recall number | F-1815-2018 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Confidence Inc./Confidence U.S.A. Inc., Port Washington, NY, United States |
| Recall initiated | 2018-07-26 |
| Classified | 2018-08-13 |
| Reported by FDA | 2018-08-22 |
| Terminated | 2019-10-22 |
| Distributed | Nationwide (US) |
| Quantity | 5,650 bottles |
| Reason classes | undeclared allergen |
| UPC / GTIN / UDI-DI | 00810891020564 |
| Lot numbers | 110516 |
Product
FP0692, Confidence, Prenatal Multi-V + DHA, 90 tablets per bottle, UPC# 8 10891 02056 4
Reason for recall
Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol (PEG), Triacetin, FD&C Yellow #6 (Sunset Yellow FCF), FD&C Red #40 (Allura Red AC), FD&C Yellow #5 (Tartrazine), and FD&C Blue #2 (Indigotine).
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-1815-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.