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Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Posted November 19, 2016
GNC Women's Multi Recalled Due to Undeclared Allergen
People who have an allergy to milk should not consume this product as it could cause a serious or life-threatening allergic reaction.
Recalled GNC Women's Ultra Mega Time Release was distributed starting in August 23, 2016 through the present. It is packaged in 180 count an HDPE plastic bottle with a child resistant closure and can be identified by the following:
- Lot# 3044FQ2024
- UPC 048107158910
- Expiration date June 2018
No other GNC brand products or lots are part of the recall.
In 2015, ConsumerLab.com tested a 90 count GNC Women's Ultra Mega Time Release multivitamin as part of its Multivitamin/Multimineral Review. However, note that the product reviewed by ConsumerLab.com is not being recalled. The recalled product is 180 count and was distributed nine months after the review.
See Related Warnings:
Immune Supplement Recalled Due To Undeclared Milk
Whey Protein Supplements Recalled Due To Undeclared Allergens
Four Probiotic Products in Canada May Pose Serious Health Risks to Those with Milk or Soy Allergies
Protein Supplement Recalled Due To Undeclared Soy and Milk
Nutrition Bar Recalled Due To Undeclared Allergen
Nutrition Shake Recalled Due To Undeclared Allergen
Protein Drinks Recalled For Undeclared Milk Source
For more information about this recall, use the link below.
Report a Problem
If you have experienced an unexpected and adverse reaction to a dietary supplement, nutritional product, or generic drug, we would like to hear about it, as we may investigate the problem. Please select from one of these options:
Dietary Supplement or Nutritional Product Problem Report
If you believe that a dietary supplement (e.g., vitamin, mineral, or herbal supplement) or other nutritional product has caused an unexpected, adverse reaction, we would like to know about it. We are collecting and organizing this information and may publish it. We might test the product in the future. You may also want to report the problem to the U.S. FDA through their Safety Reporting Portal at https://www.safetyreporting.hhs.gov.
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Generic Drug Problem Report
If you believe that a generic drug has not acted like the original drug, we would like to know about it. We are collecting and organizing this information and may publish it. We might test the product in the future. You may also want to report the problem to the U.S. FDA through their MedWatch program at the FDA MedWatch website.
Please complete the form below as accurately as possible. You may need to check the label on the drug.
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