CLASS II Food recall · Reported 22 Mar 2023 · FDA Enforcement Report

Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods recalled

Keurig DR Pepper is recalling Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods, distributed in 42 states. The recall was initiated on 3 Feb 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesUPC 099555147353 BEST BY 26 DEC 2024 LA hh:mm PL084 2360 or 2361
Quantity recalled1,844 - 24 ct sleeves

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0583-2023
FDA event ID
91651
Recalling firm
Keurig DR Pepper, Burlington, MA
Classification
Class II
Status
Terminated
Recall initiated
3 Feb 2023
FDA classified
13 Mar 2023
Reported
22 Mar 2023
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Allergens
Product category
Herbal Supplements

Timeline

3 Feb 2023Recall initiated by company
13 Mar 2023Classified by FDA+38 days
22 Mar 2023Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product contains black tea, resulting in caffeine being undeclared.

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods; packed 24 to a box

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.

AlabamaArkansasArizonaCaliforniaColoradoFloridaGeorgiaIowaIdahoIllinoisIndianaKansasKentuckyLouisianaMassachusettsMarylandMaineMichiganMinnesotaMissouri

Questions about this recall

Why was it recalled?

Product contains black tea, resulting in caffeine being undeclared.

Which lots are affected?

UPC 099555147353 BEST BY 26 DEC 2024 LA hh:mm PL084 2360 or 2361

Where was it sold?

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 it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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