Recalls / Class II
Class IIF-1815-2018
Product
FP0692, Confidence, Prenatal Multi-V + DHA, 90 tablets per bottle, UPC# 8 10891 02056 4
- Type
- Food
- Affected lot / code info
- Lot# 110516
- Quantity
- 5,650 bottles in US distribution (total for all products)
Why it was recalled
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).
Recalling firm
- Firm
- Confidence Inc./Confidence U.S.A. Inc.
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- 138 Haven Ave Ste 101, Port Washington, New York 11050-3924
Distribution
- Distribution pattern
- Nationwide
Timeline
- Recall initiated
- 2018-07-26
- FDA classified
- 2018-08-13
- Posted by FDA
- 2018-08-22
- Terminated
- 2019-10-22
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-1815-2018. The FDA issues recall classifications as health-hazard assessments, not legal findings.