Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported September 12, 2012
Stewart's Diet Orange N' Cream Soda, 12oz glass bottles
Incorrectly placed ingredient label for non-diet beverage on bottles of diet beverage. The ingredient label incorrectly provided the ingredients for regular Stewart's Orange N' C…
Dr Pepper/ Seven Up, Inc recalled Stewart's Diet Orange N' Cream Soda, 12oz glass bottles - a moderate-severity action.
Stewart's Diet Orange N' Cream Soda, 12oz glass bottles was recalled by Dr Pepper/ Seven Up, Inc in September 12, 2012. Reason: Incorrectly placed ingredient label for non-diet beverage on bottles of diet beverage. The ingredient label …. Check the official notice for the remedy. Verify recall #F-2127-2012 with the FDA Food before acting.
The recall
Dr Pepper/ Seven Up, Inc issued this moderate-severity FDA Food recall-Incorrectly placed ingredient label for non-diet beverage on bottles of diet beverage. The ingredient label ….
- Moderate
- severity level
- Class II
- classification
- September 12, 2012
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-2127-2012 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-2127-2012) was formally reported on September 12, 2012, with the manufacturer initiating the action on January 3, 2012. It is classified under Moderate severity (Class II), with a current status of Terminated. Dr Pepper/ Seven Up, Inc is listed as the recalling firm, operating out of Plano, TX. Federal records list the affected scope as 710 cases.
The documented reason for this recall is: Incorrectly placed ingredient label for non-diet beverage on bottles of diet beverage. The ingredient label incorrectly provided the ingredients for regular Stewart's Orange N' Cream Soda. The front label on the glass… Distribution data in the federal record shows the product reached: Product was distributed within the US to IL, NJ, and NY.. 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.
Food recalls over time
Where this recall sits in its category - 25,126 food 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
710 cases
Related Recalls
6
2 from same agency
Product description
Stewart's Diet Orange N' Cream Soda, 12oz glass bottles
Reason for recall
Incorrectly placed ingredient label for non-diet beverage on bottles of diet beverage. The ingredient label incorrectly provided the ingredients for regular Stewart's Orange N' Cream Soda. The front label on the glass bottles and the 4 carrier secondary package correctly identified the product as Stewart's Diet Orange N' Cream Soda.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-2127-2012 |
| Date reported | September 12, 2012 |
| Date initiated | January 3, 2012 |
| Recalling firm | Dr Pepper/ Seven Up, Inc |
| Firm location | Plano, TX |
| Affected scope | 710 cases |
| Distribution | Product was distributed within the US to IL, NJ, and NY. |
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-2127-2012) 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? ▼
Stewart's Diet Orange N' Cream Soda, 12oz glass bottles. Recalled by Dr Pepper/ Seven Up, Inc. Units affected: 710 cases.
Why was this product recalled? ▼
Incorrectly placed ingredient label for non-diet beverage on bottles of diet beverage. The ingredient label incorrectly provided the ingredients for regular Stewart's Orange N' Cream Soda. The front label on the glass bottles and the 4 carrier secondary package correctly identified the product as Stewart's Diet Orange N' Cream Soda.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on September 12, 2012. Severity: Moderate. Recall number: F-2127-2012.
Where was the recalled product distributed? ▼
Distribution: Product was distributed within the US to IL, NJ, and NY..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-2127-2012) 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
Conair Recalls Over One Million Cuisinart Grill Brushes Due to Ingestion Hazard
· 2026-07-02
CPSC Moderate
Montessori Busy Board Toys Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Sta…
Lesonic Technology Co., Ltd., dba Small Fish, of China · 2026-06-25
CPSC Moderate
Bada Boom Fireworks Recalls Pyro Diablo "Diablo Rising" Fireworks Due to Risk of Serious Injury or Death from Explosion…
· 2026-06-18
CPSC Moderate
Yamaha Recalls UMAX Bistro and Bistro Deluxe Vehicles Due to Injury Hazard
· 2026-06-11
FDA Food Critical
Butter Parsley Bagel Crisps, Item Number 18490, Net Weight: 10 lbs. Legacy Bakehouse, LLC, N8W22100 Johnson Dr., Wauk…
Legacy Bakehouse LLC · 2026-06-03
Compare this recall with Conair Recalls Over One Million Cuisinart Grill Brushes Due… →
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 12, 2012. 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.