Class IITerminated in FDA datasetRecall initiated Nov 19, 2013

PCC, Rebecca's Natural Food, Sprouts Famous Market, Ritzman Pharmacy, Earth Fare, Hartig Drug,…

Recalling firm: Nexgen Pharma, Inc.

Why it was recalled

Nexgen Pharma Inc. is recalling one lot of Woman's Once Daily vitamin because it was contaminated with the antibiotic, Chloramphenicol.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Feb 3, 2014.

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Compare the exact product and package details with the label you have.

ProductPCC, Rebecca's Natural Food, Sprouts Famous Market, Ritzman Pharmacy, Earth Fare, Hartig Drug, Viroqua Food, Ramona Fitness Center, Independent Choice (Health Trail Natural Foods-The Crunchy Grocer), Jimbo's, Outpost Natural Foods BRANDS- Woman's Once Daily Tablets - A dietary Supplement,Product Code Multivitamin/Mineral with Green Foods, Herbs, Enzymes & Probiotics Dietary Supplement. 90 Vegetarian Tablets. Manufactured for PCC Natural Markets Seattle, WA 98105

FDA code information

Lot No.: 416035

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Full FDA record and distribution details

Original product description

PCC, Rebecca's Natural Food, Sprouts Famous Market, Ritzman Pharmacy, Earth Fare, Hartig Drug, Viroqua Food, Ramona Fitness Center, Independent Choice (Health Trail Natural Foods-The Crunchy Grocer), Jimbo's, Outpost Natural Foods BRANDS- Woman's Once Daily Tablets - A dietary Supplement,Product Code Multivitamin/Mineral with Green Foods, Herbs, Enzymes & Probiotics Dietary Supplement. 90 Vegetarian Tablets. Manufactured for PCC Natural Markets Seattle, WA 98105

Extracted codes and context

TypeCode / valueContext
lot416035Lot No.: 416035

Original FDA recall reason

Nexgen Pharma Inc. is recalling one lot of Woman's Once Daily vitamin because it was contaminated with the antibiotic, Chloramphenicol.

Recall details

Recall number
F-0382-2014
Event ID
66898
FDA status
Terminated
Initiated
Nov 19, 2013
Reported
Dec 4, 2013
Classified
Nov 27, 2013
Terminated
Feb 3, 2014
Quantity
88
Location
Colorado Springs, CO, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

Nationwide distribution. No foreign, military, govt, or VA consigees.

FDA source record · F-0382-2014

Data updated September 16, 2026. View official FDA data ↗

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