Recall Radar

Keurig Dr Pepper recalls Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods: allergen risk

March 22, 2023 · Keurig Dr Pepper Class II

Class IIFDA’s middle class: use of the product may cause temporary or medically reversible adverse health consequences, or the chance of serious harm is remote.
Reason for the recallProduct contains black tea, resulting in caffeine being undeclared.

Find the official FDA enforcement report

Recall at a glance

Recalling company
Keurig Dr Pepper
Location
Burlington, MA
Reported by FDA
March 22, 2023
Recall started
February 3, 2023
Risk class
Class II
Status (latest data we have)
Terminated
Type
Voluntary: Firm initiated
Category
Beverages
Reason type
Undeclared allergens

Is my product affected?

Compare your product’s name, size and lot or date codes with the list below. A recall usually covers only specific codes.

  • Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods; packed 24 to a box
    Quantity: 1,844 - 24 ct sleeves
    Codes: UPC 099555147353 BEST BY 26 DEC 2024 LA hh:mm PL084 2360 or 2361

Where it was distributed

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.

What to do

If you have this product, check the codes above. FDA recall notices often tell consumers to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information, and if you are unsure, do not eat it. If someone becomes ill after eating a recalled food, contact a healthcare professional. See FDA’s recalls and safety alerts for company announcements.

Frequently asked questions

What was recalled?

Keurig Dr Pepper recalled 1 product, including Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods; packed 24 to a box.

Why was it recalled?

Product contains black tea, resulting in caffeine being undeclared.

What does Class II mean?

FDA’s middle class: use of the product may cause temporary or medically reversible adverse health consequences, or the chance of serious harm is remote.

Where was it sold or shipped?

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.

What should I do if I have this product?

Compare the product name, size and lot or date codes with the details on this page. FDA recall notices often tell you to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information. If you are unsure, do not eat it.

More recalls from Keurig Dr Pepper

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Sources

Data provided by the U.S. Food and Drug Administration (FDA) through openFDA, shown as published and not validated by this site. This site is independent and is not affiliated with or endorsed by FDA. It covers FDA-regulated foods; meat, poultry and egg products are regulated by USDA. Do not rely on this site for medical decisions: for health concerns contact a healthcare professional, and always follow the official notice and the company’s instructions. Terms and disclaimer.