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
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot No.: 416035
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Nexgen Pharma, Inc.
- Reason for Recall:
- Nexgen Pharma Inc. is recalling one lot of Woman's Once Daily vitamin because it was contaminated with the antibiotic, Chloramphenicol.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full 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
Product Codes/Lot Numbers:
Lot No.: 416035
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-0382-2014
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