Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods; packed 24 to a box
Summary
The FDA issued a Class II for Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods; packed 24 t by KEURIG DR PEPPER. Reason: Product contains black tea, resulting in caffeine being undeclared..
Details
Source
Food Recall
External ID
F-0583-2023
Action Date
2023-03-22
Status
Terminated
Category
food
Product Description
Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods; packed 24 to a box
Lot/Code Info: UPC 099555147353 BEST BY 26 DEC 2024 LA hh:mm PL084 2360 or 2361
Quantity Affected: 1,844 - 24 ct sleeves
Reason for Recall
Product contains black tea, resulting in caffeine being undeclared.
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.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-02-03
Company
Burlington, MA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 488 food recalls issued in the same week, part of 204 food-related FDA actions this month.
KEURIG DR PEPPER has 7 FDA actions in our database, including 7 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (KEURIG DR PEPPER) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does KEURIG DR PEPPER have FDA actions?
KEURIG DR PEPPER has 7 FDA actions in our database, including 7 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0583-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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