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
- Distributed to 11 warehouses who then fu…
KEURIG DR PEPPER Recall: Product contains black tea, resulting in caffeine being undeclared.
United States
TerminatedClass II
- Company
- KEURIG DR PEPPER
- Product
- Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-c…
- Recall date
- February 3, 2023
- Terminated
- August 21, 2023
- Source
- FDA
Reason for recall
Product contains black tea, resulting in caffeine being undeclared.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods; packed 24 to a box | Not published in this source record | 1,844 - 24 ct sleeves | UPC 099555147353 BEST BY 26 DEC 2024 LA hh:mm PL084 2360 or 2361 |
Distribution
- AL
- AR
- AZ
- CA
- CO
- FL
- GA
- IA
- ID
- IL
- IN
- KS
- KY
- LA
- MA
- MD
- ME
- MI
- MN
- MO
- MS
- MT
- NC
- ND
- NE
- NH
- NJ
- NM
- NV
- NY
- OK
- OR
- SC
- SD
- TN
- TX
- UT
- VA
- WA
- WI
- WV
- WY.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0583-2023
- Event ID
- 91651
- Status
- Terminated
- Classification
- Class II
- Company
- KEURIG DR PEPPER
- Product description
- Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods; packed 24 to a box
- Quantity
- 1,844 - 24 ct sleeves
- Reason
- Product contains black tea, resulting in caffeine being undeclared.
- Recall initiation date
- February 3, 2023
- Report date
- March 22, 2023
- Classification date
- Not published in this source record
- Termination date
- August 21, 2023
- Distribution pattern
- AL, AR, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OK, OR, SC, SD, TN, TX, UT, VA, WA, WI, WV, WY.
- UPC, lot, and code information
- UPC 099555147353 BEST BY 26 DEC 2024 LA hh:mm PL084 2360 or 2361
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: KEURIG DR PEPPER
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FDA Recall United States Terminated Historical recordClass II
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- Product
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- Published
- December 8, 2021
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
KEURIG DR PEPPER
- Product
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- Published
- December 8, 2021
- 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 |
|---|---|
| Alabama | 1 |
| Arkansas | 1 |
| Arizona | 1 |
| California | 1 |
| Colorado | 1 |
| Florida | 1 |
| Georgia | 1 |
| Iowa | 1 |
| Idaho | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Kansas | 1 |
| Kentucky | 1 |
| Louisiana | 1 |
| Massachusetts | 1 |
| Maryland | 1 |
| Maine | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| Mississippi | 1 |
| Montana | 1 |
| North Carolina | 1 |
| North Dakota | 1 |
| Nebraska | 1 |
| New Hampshire | 1 |
| New Jersey | 1 |
| New Mexico | 1 |
| Nevada | 1 |
| New York | 1 |
| Oklahoma | 1 |
| Oregon | 1 |
| South Carolina | 1 |
| South Dakota | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Utah | 1 |
| Virginia | 1 |
| Washington | 1 |
| Wisconsin | 1 |
| West Virginia | 1 |
| Wyoming | 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.
