Severity
Moderate
FDA Food recall · Reported December 4, 2013
Nexgen Pharma Inc. is recalling one lot of Woman's Once Daily vitamin because it was contaminated with the antibiotic, Chloramphenicol.
Nexgen Pharma, Inc. recalled PCC, Rebecca's Natural Food, Sprouts Famous Market, Ritzman Pharmacy, Earth Fare, Hartig … - a moderate-severity action.
PCC, Rebecca's Natural Food, Sprouts Famous Market, Ritzman Pharmacy, Earth Fare, Hartig … was recalled by Nexgen Pharma, Inc. in December 4, 2013. Reason: Nexgen Pharma Inc. is recalling one lot of Woman's Once Daily vitamin because it was contaminated with the an…. Check the official notice for the remedy. Verify recall #F-0382-2014 with the FDA Food before acting.
The recall
Nexgen Pharma, Inc. issued this moderate-severity FDA Food recall-Nexgen Pharma Inc. is recalling one lot of Woman's Once Daily vitamin because it was contaminated with the an….
Sourced from official FDA Food enforcement records. Verify recall #F-0382-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-0382-2014) was formally reported on December 4, 2013, with the manufacturer initiating the action on November 19, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. Nexgen Pharma, Inc. is listed as the recalling firm, operating out of Colorado Springs, CO. Federal records list the affected scope as 88.
The documented reason for this recall is: Nexgen Pharma Inc. is recalling one lot of Woman's Once Daily vitamin because it was contaminated with the antibiotic, Chloramphenicol. Distribution data in the federal record shows the product reached: Nationwide distribution. No foreign, military, govt, or VA consigees.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 2 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 25,126 food recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
88
Related Recalls
6
2 from same agency
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
Nexgen Pharma Inc. is recalling one lot of Woman's Once Daily vitamin because it was contaminated with the antibiotic, Chloramphenicol.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-0382-2014 |
| Date reported | December 4, 2013 |
| Date initiated | November 19, 2013 |
| Recalling firm | Nexgen Pharma, Inc. |
| Firm location | Colorado Springs, CO |
| Affected scope | 88 |
| Distribution | Nationwide distribution. No foreign, military, govt, or VA consigees. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported December 4, 2013. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.