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Class II: temporary or reversible health riskTerminated

Confidence Inc./Confidence U.S.A. Fp0692 Recall

FP0692, Confidence, Prenatal Multi-V + DHA, 90 tablets per bottle

Confidence Inc./Confidence U.S.A. Inc. · Port Washington, NY

Risk level
Class II
Reported by FDA
Aug 22, 2018
Recall ID
F-1815-2018
Check your lot numberHow we source this data

Summary

Confidence Inc./Confidence U.S.A. recalled Fp0692 starting Jul 26, 2018. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-1815-2018 on Aug 22, 2018. Reason: 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). Status: Terminated.

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).

Product description

FP0692, Confidence, Prenatal Multi-V + DHA, 90 tablets per bottle, UPC# 8 10891 02056 4

Lot numbers, UPCs & expiration codes

Lot# 110516

Where it was sold

Nationwide

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1815-2018
Classification
Class II
Status
Terminated
Recall initiated
Jul 26, 2018
FDA report date
Aug 22, 2018
Quantity
5,650 bottles in US distribution (total for all products)
Recall type
Voluntary: Firm initiated
Recalling firm
Confidence Inc./Confidence U.S.A. Inc.

Original FDA data

Every field from FDA enforcement report F-1815-2018, exactly as published.

Show all FDA fields
City
Port Washington
State
NY
Status
Terminated
Country
United States
Event ID
80620
Address
138 Haven Ave Ste 101
Code information
Lot# 110516
Postal code
11050-3924
Report date
Aug 22, 2018
Product type
Food
Recall number
F-1815-2018
Classification
Class II
Recalling firm
Confidence Inc./Confidence U.S.A. Inc.
Product quantity
5,650 bottles in US distribution (total for all products)
Termination date
Oct 22, 2019
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).
Voluntary / mandated
Voluntary: Firm initiated
Product description
FP0692, Confidence, Prenatal Multi-V + DHA, 90 tablets per bottle, UPC# 8 10891 02056 4
Distribution pattern
Nationwide
Recall initiation date
Jul 26, 2018
Initial firm notification
Letter
Center classification date
Aug 13, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1815-2018, published Aug 22, 2018. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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