RXBAR: 12-Bar Variety Pack (Chocolate Sea Salt, Peanut Butter Chocolate), and 16-Bar Variety Pack (Chocolate Sea Salt, Peanut Butter Choc...
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0894-2019.
Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties of bars due to undeclared allergen peanut.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0894-2019.
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 Chicago Bar Company Llc Rxbar 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-0894-2019.
CHICAGO BAR COMPANY LLC RXBAR
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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.
Chicago Bar Company Llc Rxbar Recall FAQ
Chicago Bar Company Llc Rxbar is the subject of a dairy safety report: RXBAR: 12-Bar Variety Pack (Chocolate Sea Salt, Peanut Butter Chocolate), and 16-Bar Variety Pack (Chocolate Sea Salt, Peanut Butter Choc.... The notice was published on December 19, 2018 by the U.S. Food and Drug Administration (FDA). Approximately 75,695,266 units are potentially affected.