Severity
Moderate
FDA Food recall · Reported October 24, 2012
Dr Pepper/Seven Up, Inc. has initiated a recall of mislabeled Diet Crush Orange Soda produced under license issued by one of their licensed bottlers, Pepsi Beverages Company in Ph…
Bottling LLC dba Pepsi Beverages Company recalled Diet Crush Orange Soda, 12 oz cans - a moderate-severity action.
Diet Crush Orange Soda, 12 oz cans was recalled by Bottling LLC dba Pepsi Beverages Company in October 24, 2012. Reason: Dr Pepper/Seven Up, Inc. has initiated a recall of mislabeled Diet Crush Orange Soda produced under license i…. Check the official notice for the remedy. Verify recall #F-0121-2013 with the FDA Food before acting.
The recall
Bottling LLC dba Pepsi Beverages Company issued this moderate-severity FDA Food recall-Dr Pepper/Seven Up, Inc. has initiated a recall of mislabeled Diet Crush Orange Soda produced under license i….
Sourced from official FDA Food enforcement records. Verify recall #F-0121-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-0121-2013) was formally reported on October 24, 2012, with the manufacturer initiating the action on February 5, 2012. It is classified under Moderate severity (Class II), with a current status of Terminated. Bottling LLC dba Pepsi Beverages Company is listed as the recalling firm, operating out of Phoenix, AZ. Federal records list the affected scope as 1791 cases.
The documented reason for this recall is: Dr Pepper/Seven Up, Inc. has initiated a recall of mislabeled Diet Crush Orange Soda produced under license issued by one of their licensed bottlers, Pepsi Beverages Company in Phoenix, Arizona. The bottler used new gr… Distribution data in the federal record shows the product reached: Arizona. 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.
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.
Severity
Moderate
Affected scope
1791 cases
Related Recalls
6
2 from same agency
Diet Crush Orange Soda, 12 oz cans
Dr Pepper/Seven Up, Inc. has initiated a recall of mislabeled Diet Crush Orange Soda produced under license issued by one of their licensed bottlers, Pepsi Beverages Company in Phoenix, Arizona. The bottler used new graphics on cans of product made with the previous formulation which is in the process of being discontinued.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-0121-2013 |
| Date reported | October 24, 2012 |
| Date initiated | February 5, 2012 |
| Recalling firm | Bottling LLC dba Pepsi Beverages Company |
| Firm location | Phoenix, AZ |
| Affected scope | 1791 cases |
| Distribution | Arizona |
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.
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.
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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 October 24, 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.