FDA Recall United States Terminated Historical recordClass II
Swire Coca Cola USA
- Product
- Coca-Cola Cherry Zero Sugar Fridge Pack, 12 - 12 FL OZ CANS…
- Published
- March 16, 2022
- Distribution
- Multiple states
Swire Coca Cola USA Recall: Swire Coca Cola is recalling certain Diet Dr Pepper bottle due to the potential presence of foreign material.
United States
TerminatedClass II
- Company
- Swire Coca Cola USA
- Product
- Dr. Pepper Est. 1885 Diet, 20 FL Oz (1.25 PT), 591 mL
- Recall date
- March 21, 2018
- Terminated
- July 30, 2018
- Source
- FDA
Reason for recall
Swire Coca Cola is recalling certain Diet Dr Pepper bottle due to the potential presence of foreign material.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Dr. Pepper Est. 1885 Diet, 20 FL Oz (1.25 PT), 591 mL | Not published in this source record | 366 cases | Date Code: JUN1818TOA |
Distribution
- Nationwide. No foreign/VA/govt/military accounts
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1114-2018
- Event ID
- 79618
- Status
- Terminated
- Classification
- Class II
- Company
- Swire Coca Cola USA
- Product description
- Dr. Pepper Est. 1885 Diet, 20 FL Oz (1.25 PT), 591 mL
- Quantity
- 366 cases
- Reason
- Swire Coca Cola is recalling certain Diet Dr Pepper bottle due to the potential presence of foreign material.
- Recall initiation date
- March 21, 2018
- Report date
- April 25, 2018
- Classification date
- Not published in this source record
- Termination date
- July 30, 2018
- Distribution pattern
- Nationwide. No foreign/VA/govt/military accounts
- UPC, lot, and code information
- Date Code: JUN1818TOA
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Swire Coca Cola USA
Other recalls from Swire Coca Cola USA
FDA Recall United States Terminated Historical recordClass III
Swire Coca Cola USA
- Product
- Caffeine-Free Barq s Root Beer 12 Pack, 12 oz cans
- Published
- October 3, 2018
- Distribution
- Nationwide
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Virginia | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
