Safety Report: GNC Women's 30+ Vitapak recalled due to Undeclared Fish Allergen, USA
1 week ago •source accessdata.fda.gov
Recall notice
United States
GNC Holdings LLC has issued a recall for its Women's 30+ Vitapak due to an undeclared fish allergen, parvalbumin. The product was distributed across multiple states including AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, TN, TX, UT, VA, WA, WI, WV, WY.The recall was initiated on April 25, 2025, and was classified as Class III by the FDA on June 5, 2025.
The recall involves:
- Name: GNC Women’s 30+ Vitapak
- Packaging: Carton of 30 sachets; each sachet contains four tablets and one capsule
- Lot Numbers:
1060EB2401, 1060EB2402, 1060EB2403, 1060EB2404, 1060EB2405, 1060EB2501, 1060EB2502, 1060EB2503
- Package Dimensions: 10.25” W x 3.56” H x 3.15” D
- Quantity Recalled: 144,430 units
In case you experience harm from allergens or undeclared ingredients, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Source: www.accessdata.fda.gov/scripts/ires/index.cfm
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