Thumbs Up Candy Bar. A Crunchy, Peanut Buttery Center in a a rice-milk chocolately coating, 1.3 oz, gluten-free,dairy-free & vegan, no tr...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1435-2013.
Go Max Go Foods is recalling various lots of vegan candy bar products containing the statement "dairy-free" due to undeclared milk.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1435-2013.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Go Max Go Foods or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1435-2013.
Go Max Go Foods
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Go Max Go Foods Recall FAQ
Go Max Go Foods is the subject of a dairy safety report: Thumbs Up Candy Bar. A Crunchy, Peanut Buttery Center in a a rice-milk chocolately coating, 1.3 oz, gluten-free,dairy-free & vegan, no tr.... The notice was published on April 22, 2013 by the U.S. Food and Drug Administration (FDA). Approximately 16,236 units are potentially affected.