CLASS III Food recall · Reported 8 Apr 2026 · FDA Enforcement Report

Popping Boba Rtd Mixed Berry Hibiscus Tea recalled

Pocas International is recalling Popping Boba Rtd Mixed Berry Hibiscus Tea, distributed in 8 states. The recall was initiated on 16 Mar 2026 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesWill be provided by firm
Quantity recalled148 Cases

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
H-0634-2026
FDA event ID
98585
Recalling firm
Pocas International, S Hackensack, NJ
Classification
Class III
Status
Terminated
Recall initiated
16 Mar 2026
FDA classified
27 Mar 2026
Reported
8 Apr 2026
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Packaging Defects
Product category
Tea

Timeline

16 Mar 2026Recall initiated by company
27 Mar 2026Classified by FDA+11 days
8 Apr 2026Published in enforcement report+12 days

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

Reason for recall

Packaging integrity issue that may compromise product quality .

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

POPPING BOBA RTD MIXED BERRY HIBISCUS TEA 12 X 13.8OZ

Where it was distributed

The product was distributed to the following states: NY, VA, FL, MA, TX, LA, UT, CA and Canada

CaliforniaFloridaLouisianaMassachusettsNew YorkTexasUtahVirginia

Questions about this recall

Why was it recalled?

Packaging integrity issue that may compromise product quality .

Which lots are affected?

Will be provided by firm

Where was it sold?

The product was distributed to the following states: NY, VA, FL, MA, TX, LA, UT, CA and Canada

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

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.

Other products in this recall event

3 other products · FDA event 98585

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