CLASS III Food recall · Reported 11 Jun 2025 · FDA Enforcement Report
GNC Women's 30+ Vitapak, Carton of 30 Sachets recalled by GNC Holdings
GNC Holdings is recalling GNC Women's 30+ Vitapak, Carton of 30 Sachets, distributed in 48 states. The recall was initiated on 25 Apr 2025 and the FDA has classified it as Class III.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0928-2025
- FDA event ID
- 96759
- Recalling firm
- GNC Holdings, Pittsburgh, PA
- Brand
- GNC Women's
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 25 Apr 2025
- FDA classified
- 5 Jun 2025
- Reported
- 11 Jun 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Undeclared Fish & Shellfish
- Product category
- Other
Timeline
| 25 Apr 2025 | Recall initiated by company | |
| 5 Jun 2025 | Classified by FDA | +41 days |
| 11 Jun 2025 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Undeclared Fish allergen (parvalbumin).
Product as listed by the FDA
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
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
AlabamaArkansasArizonaCaliforniaColoradoConnecticutDistrict of ColumbiaDelawareFloridaGeorgiaHawaiiIowaIdahoIllinoisIndianaKansasKentuckyLouisianaMassachusettsMaryland
Questions about this recall
Why was it recalled?
Undeclared Fish allergen (parvalbumin).
Which lots are affected?
Lot No. 1060EB2401 1060EB2402 1060EB2403 1060EB2404 1060EB2405 1060EB2501 1060EB2502 1060EB2503
Where was it 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 should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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