Recall Radar

GNC Holdings recalls GNC Women's 30+ Vitapak: allergen risk

June 11, 2025 · GNC Holdings Class III

Class IIIFDA’s lowest-risk class: use of the product is not likely to cause adverse health consequences.
Reason for the recallUndeclared Fish allergen (parvalbumin).

Find the official FDA enforcement report

Recall at a glance

Recalling company
GNC Holdings
Location
Pittsburgh, PA
Reported by FDA
June 11, 2025
Recall started
April 25, 2025
Risk class
Class III
Status (latest data we have)
Terminated
Type
Voluntary: Firm initiated
Category
Supplements and infant formula
Reason type
Undeclared allergens

Is my product affected?

Compare your product’s name, size and lot or date codes with the list below. A recall usually covers only specific codes.

  • 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
    Codes: Lot No. 1060EB2401 1060EB2402 1060EB2403 1060EB2404 1060EB2405 1060EB2501 1060EB2502 1060EB2503

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

What to do

If you have this product, check the codes above. FDA recall notices often tell consumers to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information, and if you are unsure, do not eat it. If someone becomes ill after eating a recalled food, contact a healthcare professional. See FDA’s recalls and safety alerts for company announcements.

Frequently asked questions

What was recalled?

GNC Holdings recalled 1 product, including GNC Women's 30+ Vitapak, Carton of 30 Sachets. Each sachet contains four tablets and a capsule. Paper-board carton that measures 10.25….

Why was it recalled?

Undeclared Fish allergen (parvalbumin).

What does Class III mean?

FDA’s lowest-risk class: use of the product is not likely to cause adverse health consequences.

Where was it sold or shipped?

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

What should I do if I have this product?

Compare the product name, size and lot or date codes with the details on this page. FDA recall notices often tell you to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information. If you are unsure, do not eat it.

Similar recalls in supplements and infant formula

Sources

Data provided by the U.S. Food and Drug Administration (FDA) through openFDA, shown as published and not validated by this site. This site is independent and is not affiliated with or endorsed by FDA. It covers FDA-regulated foods; meat, poultry and egg products are regulated by USDA. Do not rely on this site for medical decisions: for health concerns contact a healthcare professional, and always follow the official notice and the company’s instructions. Terms and disclaimer.