Recalling firm
GNC Holdings LLC
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2025-06-11
Distribution
The adulterated product was distributed to the various states: 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
Firm state
PA
Product quantity
144,430 Units
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Documentation & Change ControlReason for recall
Undeclared Fish allergen (parvalbumin).
Product description
GNC Women's 30+ Vitapak, Carton of 30 Sachets. Each sachet contains four tablets and a capsule. Paper-board carton that measures 10.25 width x 3.56 height x 3.15 depth containing 30 sachets of 3 width x 2.75 height with tear notch. 15 Cartons per Case
Code / lot info
Lot No. 1060EB2401 1060EB2402 1060EB2403 1060EB2404 1060EB2405 1060EB2501 1060EB2502 1060EB2503
Other recalls SPEQ maps to Documentation & Change Control
See all Documentation & Change Control recalls →Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.