Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported October 12, 2016
Diet Dr Pepper, 12 oz. can/24 pack, UPC 078000083132; Diet Dr Pepper, 12 oz. can/6 pack, UPC N/A; Diet Dr Pepper, 12 oz. can/20 pack, UPC 078000083095; Dr Pepper, 12 oz. can/6 pack, UPC N/A; Dr Pepper , 12 oz. can/ 20 pack, UPC 078000082098; Dr Pepper 12 oz. can/ 12 pack, UPC 078000082166; Dr Pepper, 12 oz. can/24 pack, UPC 078000082135
In a small percentage of the cans, when opened, the oval covering for the hole, which normally is pushed down into the can, instead opens upward. This produces a loud "pop" sound…
Compiled from official public sources by the editorial team.
Verify with FDA Food →
Coca-Cola Company (The) recalled Diet Dr Pepper, 12 oz. can/24 pack, UPC 078000083132; Diet Dr Pepper, 12 oz. can/6 pack, … - a moderate-severity action.
Diet Dr Pepper, 12 oz. can/24 pack, UPC 078000083132; Diet Dr Pepper, 12 oz. can/6 pack, … was recalled by Coca-Cola Company (The) in October 12, 2016. Reason: In a small percentage of the cans, when opened, the oval covering for the hole, which normally is pushed down…. Check the official notice for the remedy. Verify recall #F-2643-2016 with the FDA Food before acting.
The recall
Coca-Cola Company (The) issued this moderate-severity FDA Food recall-In a small percentage of the cans, when opened, the oval covering for the hole, which normally is pushed down….
- Moderate
- severity level
- Class II
- classification
- October 12, 2016
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-2643-2016 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-2643-2016) was formally reported on October 12, 2016, with the manufacturer initiating the action on April 29, 2016. It is classified under Moderate severity (Class II), with a current status of Terminated. Coca-Cola Company (The) is listed as the recalling firm, operating out of Atlanta, GA. Federal records list the affected scope as 14,168 cases total.
The documented reason for this recall is: In a small percentage of the cans, when opened, the oval covering for the hole, which normally is pushed down into the can, instead opens upward. This produces a loud "pop" sound. Recall initiated on 4/29/16. Distribution data in the federal record shows the product reached: AZ, OR, & WA. 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
14,168 cases total
Related Recalls
6
2 from same agency
Product description
Diet Dr Pepper, 12 oz. can/24 pack, UPC 078000083132; Diet Dr Pepper, 12 oz. can/6 pack, UPC N/A; Diet Dr Pepper, 12 oz. can/20 pack, UPC 078000083095; Dr Pepper, 12 oz. can/6 pack, UPC N/A; Dr Pepper , 12 oz. can/ 20 pack, UPC 078000082098; Dr Pepper 12 oz. can/ 12 pack, UPC 078000082166; Dr Pepper, 12 oz. can/24 pack, UPC 078000082135
Reason for recall
In a small percentage of the cans, when opened, the oval covering for the hole, which normally is pushed down into the can, instead opens upward. This produces a loud "pop" sound. Recall initiated on 4/29/16.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-2643-2016 |
| Date reported | October 12, 2016 |
| Date initiated | April 29, 2016 |
| Recalling firm | Coca-Cola Company (The) |
| Firm location | Atlanta, GA |
| Affected scope | 14,168 cases total |
| Distribution | AZ, OR, & WA |
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-2643-2016) 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? ▼
Diet Dr Pepper, 12 oz. can/24 pack, UPC 078000083132; Diet Dr Pepper, 12 oz. can/6 pack, UPC N/A; Diet Dr Pepper, 12 oz. can/20 pack, UPC 078000083095; Dr Pepper, 12 oz. can/6 pack, UPC N/A; Dr Pepper , 12 oz. can/ 20 pack, UPC 078000082098; Dr Pepper 12 oz. can/ 12 pack, UPC 078000082166; Dr Pepper, 12 oz. can/24 pack, UPC 078000082135. Recalled by Coca-Cola Company (The). Units affected: 14,168 cases total.
Why was this product recalled? ▼
In a small percentage of the cans, when opened, the oval covering for the hole, which normally is pushed down into the can, instead opens upward. This produces a loud "pop" sound. Recall initiated on 4/29/16.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on October 12, 2016. Severity: Moderate. Recall number: F-2643-2016.
Where was the recalled product distributed? ▼
Distribution: AZ, OR, & WA.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-2643-2016) 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.
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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 12, 2016. 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.