GNC Women's 30+ Vitapak recall
Recalled by GNC Holdings LLC · Pittsburgh, PA, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Undeclared Fish allergen (parvalbumin).
Undeclared allergen: Fish
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
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
Quantity: 144,430 Units
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot No. 1060EB2401 1060EB2402 1060EB2403 1060EB2404 1060EB2405 1060EB2501 1060EB2502 1060EB2503
Where it was sold
Alabama Arkansas Arizona California Colorado Connecticut District of Columbia Delaware Florida Georgia Hawaii Iowa Idaho Illinois Indiana Kansas Kentucky Louisiana Massachusetts Maryland Maine Michigan Minnesota Missouri Mississippi North Carolina North Dakota Nebraska New Hampshire New Jersey New Mexico Nevada New York Ohio Oklahoma Oregon Pennsylvania Puerto Rico Rhode Island South Carolina Tennessee Texas Utah Virginia Washington Wisconsin West Virginia Wyoming
FDA's distribution note: 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
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. The risk from an undeclared allergen is to people allergic to fish; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- GNC Holdings LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Apr 25, 2025
- In FDA report of
- Jun 11, 2025
- Terminated
- Jun 17, 2025
- FDA recall number
- F-0928-2025 · event 96759
- Official record
- FDA enforcement report search