Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported April 25, 2018
Dr. Pepper Est. 1885 Diet, 20 FL Oz (1.25 PT), 591 mL
Swire Coca Cola is recalling certain Diet Dr Pepper bottle due to the potential presence of foreign material.
Swire Coca Cola USA recalled Dr. Pepper Est. 1885 Diet, 20 FL Oz (1.25 PT), 591 mL — a moderate-severity action.
Dr. Pepper Est. 1885 Diet, 20 FL Oz (1.25 PT), 591 mL was recalled by Swire Coca Cola USA in April 25, 2018. Reason: Swire Coca Cola is recalling certain Diet Dr Pepper bottle due to the potential presence of foreign material.. Check the official notice for the remedy. Verify recall #F-1114-2018 with the FDA Food before acting.
The recall
Swire Coca Cola USA issued this moderate-severity FDA Food recall — Swire Coca Cola is recalling certain Diet Dr Pepper bottle due to the potential presence of foreign material..
- Moderate
- severity level
- Class II
- classification
- April 25, 2018
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-1114-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-1114-2018) was formally reported on April 25, 2018, with the manufacturer initiating the action on March 21, 2018. It is classified under Moderate severity (Class II), with a current status of Terminated. Swire Coca Cola USA is listed as the recalling firm, operating out of West Valley City, UT. Federal records list the affected scope as 366 cases.
The documented reason for this recall is: Swire Coca Cola is recalling certain Diet Dr Pepper bottle due to the potential presence of foreign material. Distribution data in the federal record shows the product reached: Nationwide. No foreign/VA/govt/military accounts. 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, 6 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.
Children & Baby Products recalls over time
Where this recall sits in its category — 3,146 children & baby products recalls on record
Where this recall sits in the database
Of 100,165 recalls in the database, 23,668 are high severity, 72,097 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
366 cases
Related Recalls
6
6 from same agency
Product description
Dr. Pepper Est. 1885 Diet, 20 FL Oz (1.25 PT), 591 mL
Reason for recall
Swire Coca Cola is recalling certain Diet Dr Pepper bottle due to the potential presence of foreign material.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-1114-2018 |
| Date reported | April 25, 2018 |
| Date initiated | March 21, 2018 |
| Recalling firm | Swire Coca Cola USA |
| Firm location | West Valley City, UT |
| Affected scope | 366 cases |
| Distribution | Nationwide. No foreign/VA/govt/military accounts |
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-1114-2018) 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? ▼
Dr. Pepper Est. 1885 Diet, 20 FL Oz (1.25 PT), 591 mL. Recalled by Swire Coca Cola USA. Units affected: 366 cases.
Why was this product recalled? ▼
Swire Coca Cola is recalling certain Diet Dr Pepper bottle due to the potential presence of foreign material.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on April 25, 2018. Severity: Moderate. Recall number: F-1114-2018.
Where was the recalled product distributed? ▼
Distribution: Nationwide. No foreign/VA/govt/military accounts.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-1114-2018) 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.
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What to do next
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Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.
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Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported April 25, 2018.
- Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
- Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
- Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records — no number is typed in by an editor. 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 June 2026.