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FDA recall, , Low risk

Popping Boba RTD Tea

Popping Boba RTD teas have a packaging integrity issue that may compromise product quality.

Recall ended Apr 16, 2026. Still check yours.

What happened

Pocas International Corp. of S Hackensack, New Jersey, recalled four Popping Boba RTD teas because of a packaging integrity issue that may compromise product quality. The products include Mixed Berry Hibiscus Tea, Peach Oolong Tea, Strawberry Dragon F/Oolong Tea, and Mango Passion Fruit Green Tea. The recall began March 16, 2026, and was added to the FDA's Enforcement Report on March 27, 2026.

The teas were distributed in New York, Virginia, Florida, Massachusetts, Texas, Louisiana, Utah, California, and Canada.

What to do

We don't have product-specific instructions for this recall. FDA's general advice for food recalls:

  1. Return it to the store where you bought it, or throw it away.
  2. Don't give it to anyone else, such as a food bank, or to a pet.

Is yours affected?

4 products

Compare these details with yours, then check the recall notice to see which units are recalled.

  1. Popping Boba RTD Mixed Berry Hibiscus Tea 12 X 13.8OZ

    Affected units
    Will be provided by firm
  2. Popping Boba RTD Peach Oolong Tea 12 X 13.8OZ

    Affected units
    Will be provided by firm
  3. Popping Boba RTD Strawberry Dragon F/Oolong Tea 12 X 13.8OZ

    Affected units
    Will be provided by firm
  4. Popping Boba RTD Mango Passion Fruit Green Tea 12 X 13.8OZ

    Affected units
    Will be provided by firm

Recall details

Company began the recall
Sold in

The product was distributed to the following states: New York, Virginia, Florida, Massachusetts, Texas, Louisiana, Utah, California and Canada

Company
Pocas International Corp.S Hackensack, New Jersey
Risk

Low risk

Eating it is unlikely to cause health problems.

FDA Class III recall · How risk is rated

Event ID
98585
Recall numbers
H-0633-2026 to H-0636-2026

Timeline

FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.

  1. Company began the recall

  2. Added to FDA's Enforcement Report · Classified by FDA

  3. In FDA's weekly enforcement report

  4. Recall ended

  5. Listed on Recall Canary

  6. Archived

  7. Summary updated

Summary by Recall Canary, written with AI · summary updated Oct 2, 2026 · primary source: U.S. Food and Drug Administration (opens in a new tab)