GNC Women's 30+ Vitapak, Carton of 30 Sachets. Each sachet contains four tablets and a capsule.…
Recalling firm: GNC Holdings LLC
Undeclared Fish allergen (parvalbumin).
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jun 17, 2025.
Check your package
Compare the exact product and package details with the label you have.
FDA code information
Lot No. 1060EB2401 1060EB2402 1060EB2403 1060EB2404 1060EB2405 1060EB2501 1060EB2502 1060EB2503
Match the product, package size, and code together. A missing match does not guarantee safety.
Full FDA record and distribution details
Original 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
Original FDA recall reason
Undeclared Fish allergen (parvalbumin).
Recall details
- Recall number
- F-0928-2025
- Event ID
- 96759
- FDA status
- Terminated
- Initiated
- Apr 25, 2025
- Reported
- Jun 11, 2025
- Classified
- Jun 5, 2025
- Terminated
- Jun 17, 2025
- Quantity
- 144,430 Units
- Location
- Pittsburgh, PA, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
Where it was distributed
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
Data updated September 16, 2026. View official FDA data ↗
Follow official FDA and manufacturer guidance.