Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported September 9, 2015
A&W Cream Soda 12 FL OZ (355 mL)
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
Compiled from official public sources by the editorial team.
Verify with FDA Food →
Dr. Pepper Snapple Group Inc recalled A&W Cream Soda 12 FL OZ (355 mL) - a moderate-severity action.
A&W Cream Soda 12 FL OZ (355 mL) was recalled by Dr. Pepper Snapple Group Inc in September 9, 2015. Reason: The American Bottling Company is recalling 12 oz. cans of A& W Cream Soda because the front panel bears the s…. Check the official notice for the remedy. Verify recall #F-3079-2015 with the FDA Food before acting.
The recall
Dr. Pepper Snapple Group Inc issued this moderate-severity FDA Food recall-The American Bottling Company is recalling 12 oz. cans of A& W Cream Soda because the front panel bears the s….
- Moderate
- severity level
- Class II
- classification
- September 9, 2015
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-3079-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-3079-2015) was formally reported on September 9, 2015, with the manufacturer initiating the action on August 4, 2015. It is classified under Moderate severity (Class II), with a current status of Terminated. Dr. Pepper Snapple Group Inc is listed as the recalling firm, operating out of Plano, TX. Federal records list the affected scope as 10,292 cases (12 cans/case).
The documented reason for this recall is: 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 Distribution data in the federal record shows the product reached: U.S. distribution to the following; CA, NV, and ID. No foreign consignees.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 2 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Cosmetics & Personal Care recalls over time
Where this recall sits in its category - 1,360 cosmetics & personal care recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
10,292 cases (12 cans/case)
Related Recalls
6
2 from same agency
Product description
A&W Cream Soda 12 FL OZ (355 mL)
Reason for recall
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
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-3079-2015 |
| Date reported | September 9, 2015 |
| Date initiated | August 4, 2015 |
| Recalling firm | Dr. Pepper Snapple Group Inc |
| Firm location | Plano, TX |
| Affected scope | 10,292 cases (12 cans/case) |
| Distribution | U.S. distribution to the following; CA, NV, and ID. No foreign consignees. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-3079-2015) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
A&W Cream Soda 12 FL OZ (355 mL). Recalled by Dr. Pepper Snapple Group Inc. Units affected: 10,292 cases (12 cans/case).
Why was this product recalled? ▼
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
Which agency issued this recall? ▼
This recall was issued by the FDA Food on September 9, 2015. Severity: Moderate. Recall number: F-3079-2015.
Where was the recalled product distributed? ▼
Distribution: U.S. distribution to the following; CA, NV, and ID. No foreign consignees..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-3079-2015) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
CPSC Moderate
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PS Seasoning & Spices, Inc. · 2026-05-27
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VG7274D1 Natural Cream of Mushroom Type Flavor, Net Weight: 50 lbs. bag. Item #: R5302. For Further Processing. …
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FDA Drug Critical
MG217 Multi-Symptom Treatment Cream & Skin Protectant (colloidal oatmeal 2%), NET WT 6 oz (170 g), Manufactured by: Pha…
Wisconsin Pharmacal Company · 2026-05-27
FDA Drug Moderate
Fluocinonide, USP, 0.05% Cream, 30g tube, Rx only, Mfd by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1…
SUN PHARMACEUTICAL INDUSTRIES INC · 2026-04-22
Compare this recall with Tiny Land Children's Play Tents Recalled Due to Risk of Inj… →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported September 9, 2015. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.