Class IIIFood recall: undeclared fish
GNC Women's 30+ Vitapak
GNC Holdings LLC, of Pittsburgh, PA, began recalling this product on . FDA classified the recall as Class III on .
Why it was recalled
In FDA’s words:
Undeclared Fish allergen (parvalbumin).
The allergen tags on this page are ours, matched from FDA’s words above.
The product
GNC Women's 30+ Vitapak
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
- Codes and dates
- Lot No. 1060EB2401 1060EB2402 1060EB2403 1060EB2404 1060EB2405 1060EB2501 1060EB2502 1060EB2503
- Quantity
- 144,430 Units
- Recall number
- F-0928-2025
Where it was distributed
In FDA’s words:
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 Class III means
In FDA’s definitions, a Class III recall is one where: use of or exposure to the product is not likely to cause adverse health consequences. FDA’s recall definitions
If you have this product
- FDA’s enforcement report doesn’t say what to do with a recalled product. FDA posts some companies’ recall announcements on its Recalls, Market Withdrawals and Safety Alerts page; not every recall has one.
- FDA doesn’t update a recall’s status after classifying it, so this page can’t tell you whether the recall is still open.
- If someone has a serious allergic reaction, call 911. Signs of a serious reaction
Source
FDA’s Enforcement Report, read through openFDA. This recall first appeared in the report of . openFDA asks that its data not be relied on for decisions about medical care. AllergyNest isn’t affiliated with or endorsed by FDA.