Chocolate, confections. Bulk Milk BigMouth, item number 233. 8 piece per case.
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (Salmonella contamination). 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-0575-2013.
The firm voluntarily recalled 13 of its gourmet peanut butter chocolate products because they have the potential to be contaminated with Salmonella, upon learning that Sunland, Inc., the peanut butter supplier used in the production of Xan Confections, has recalled its entire peanut butter product from May 1, 2012 throught September 24, 2012.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0575-2013.
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 Xan Confections 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-0575-2013.
Xan Confections
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.
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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.
Xan Confections Recall FAQ
Xan Confections is the subject of a dairy safety report: Chocolate, confections. Bulk Milk BigMouth, item number 233. 8 piece per case.. The notice was published on October 1, 2012 by the U.S. Food and Drug Administration (FDA). Approximately 94 units are potentially affected.