Severity
Low
LowClass IIITerminated
FDA Food recall · Reported June 11, 2025
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
Undeclared Fish allergen (parvalbumin).
Gnc Holdings LLC recalled GNC Women's 30+ Vitapak, Carton of 30 Sachets. Each sachet contains four tablets and a c… - a low-severity action.
GNC Women's 30+ Vitapak, Carton of 30 Sachets. Each sachet contains four tablets and a c… was recalled by Gnc Holdings LLC in June 11, 2025. Reason: Undeclared Fish allergen (parvalbumin).. Check the official notice for the remedy. Verify recall #F-0928-2025 with the FDA Food before acting.
The recall
Gnc Holdings LLC issued this low-severity FDA Food recall-Undeclared Fish allergen (parvalbumin)..
- Low
- severity level
- 144K units
- affected scope
- Class III
- classification
- June 11, 2025
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-0928-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-0928-2025) was formally reported on June 11, 2025, with the manufacturer initiating the action on April 25, 2025. It is classified under Low severity (Class III), with a current status of Terminated. Gnc Holdings LLC is listed as the recalling firm, operating out of Pittsburgh, PA. Federal records list the affected scope as 144,430 Units, a scale large enough to require multi-state distribution tracking.
The documented reason for this recall is: Undeclared Fish allergen (parvalbumin). Distribution data in the federal record shows the product reached: 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,…. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 2 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Food recalls over time
Where this recall sits in its category - 25,126 food recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
144,430 Units
Related Recalls
6
2 from same agency
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
Reason for recall
Undeclared Fish allergen (parvalbumin).
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | F-0928-2025 |
| Date reported | June 11, 2025 |
| Date initiated | April 25, 2025 |
| Recalling firm | Gnc Holdings LLC |
| Firm location | Pittsburgh, PA |
| Affected scope | 144,430 Units |
| Distribution | 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,… |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-0928-2025) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product 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. Recalled by Gnc Holdings LLC. Units affected: 144,430 Units.
Why was this product recalled? ▼
Undeclared Fish allergen (parvalbumin).
Which agency issued this recall? ▼
This recall was issued by the FDA Food on June 11, 2025. Severity: Low. Recall number: F-0928-2025.
Where was the recalled product distributed? ▼
Distribution: 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.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0928-2025) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported June 11, 2025. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.