FDA Recall United States Terminated Historical recordClass II
KEURIG DR PEPPER
- Product
- Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-c…
- Published
- March 22, 2023
- Distribution
- AL, AR, AZ, CA, CO, FL, GA, IA, ID, IL,…
KEURIG DR PEPPER Recall: Consumer complaints of off flavor and aroma
United States
TerminatedClass II
- Company
- KEURIG DR PEPPER
- Product
- Rc Cola 12 Oz (355 mL) packaged in an aluminum can 12 can to…
- Recall date
- September 13, 2021
- Terminated
- December 8, 2021
- Source
- FDA
Reason for recall
Consumer complaints of off flavor and aroma
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Rc Cola 12 Oz (355 mL) packaged in an aluminum can 12 can to a pack | Not published in this source record | 9238 cases | production code of the product is G1211 CB3U |
Distribution
- West Virginia
- Virginia
- Ohio
- Kentucky
- Indiana
- Pennsylvania
- New Jersey
- Tennessee
- Georgia.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0008-2022
- Event ID
- 88723
- Status
- Terminated
- Classification
- Class II
- Company
- KEURIG DR PEPPER
- Product description
- Rc Cola 12 Oz (355 mL) packaged in an aluminum can 12 can to a pack
- Quantity
- 9238 cases
- Reason
- Consumer complaints of off flavor and aroma
- Recall initiation date
- September 13, 2021
- Report date
- October 6, 2021
- Classification date
- Not published in this source record
- Termination date
- December 8, 2021
- Distribution pattern
- West Virginia, Virginia, Ohio, Kentucky, Indiana, Pennsylvania, New Jersey, Tennessee, Georgia.
- UPC, lot, and code information
- production code of the product is G1211 CB3U
- 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: KEURIG DR PEPPER
Other recalls from KEURIG DR PEPPER
FDA Recall United States Terminated Historical recordClass II
KEURIG DR PEPPER
- Product
- Diet Snapple Tea Peach Tea 16 oz. packaged in PET bottle. Ex…
- Published
- January 12, 2022
- Distribution
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FDA Recall United States Terminated Historical recordClass II
KEURIG DR PEPPER
- Product
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- Published
- December 8, 2021
- Distribution
- Nationwide
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.
