A&W Cream Soda 12 FL OZ (355 mL)
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-3079-2015.
The American Bottling Company is recalling 12 oz. cans of A& W Cream Soda because the front panel bears the statement "caffeine free" and the product contains caffeine
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-3079-2015.
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 Dr. Pepper Snapple Group Inc 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-3079-2015.
Dr. Pepper Snapple Group Inc
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.
Dr. Pepper Snapple Group Inc Recall FAQ
Dr. Pepper Snapple Group Inc is the subject of a dairy safety report: A&W Cream Soda 12 FL OZ (355 mL). The notice was published on August 4, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 10,292 units are potentially affected.