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Class III: unlikely to cause harmTerminated

GNC Women's 30+ Vitapak Recall

GNC Women's 30+ Vitapak, Carton of 30 Sachets

GNC Holdings LLC · Pittsburgh, PA

Risk level
Class III
Reported by FDA
Jun 11, 2025
Recall ID
F-0928-2025
Check your lot numberHow we source this data

Summary

GNC Holdings recalled GNC Women's 30+ Vitapak starting Apr 25, 2025. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report F-0928-2025 on Jun 11, 2025. Reason: Undeclared Fish allergen (parvalbumin). Status: Terminated.

Why it was recalled

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

Lot numbers, UPCs & expiration codes

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

Where it was sold

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

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0928-2025
Classification
Class III
Status
Terminated
Recall initiated
Apr 25, 2025
FDA report date
Jun 11, 2025
Quantity
144,430 Units
Recall type
Voluntary: Firm initiated
Recalling firm
GNC Holdings LLC

Original FDA data

Every field from FDA enforcement report F-0928-2025, exactly as published.

Show all FDA fields
City
Pittsburgh
State
PA
Status
Terminated
Country
United States
Event ID
96759
Address
75 Hopper Pl
Code information
Lot No. 1060EB2401 1060EB2402 1060EB2403 1060EB2404 1060EB2405 1060EB2501 1060EB2502 1060EB2503
Postal code
15222-4733
Report date
Jun 11, 2025
Product type
Food
Recall number
F-0928-2025
Classification
Class III
Recalling firm
GNC Holdings LLC
Product quantity
144,430 Units
Termination date
Jun 17, 2025
Reason for recall
Undeclared Fish allergen (parvalbumin).
Voluntary / mandated
Voluntary: Firm initiated
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
Distribution pattern
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
Recall initiation date
Apr 25, 2025
Initial firm notification
E-Mail
Center classification date
Jun 5, 2025

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0928-2025, published Jun 11, 2025. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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