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RECALL RECORD — CLASS IIRecall closedF-1688-2012/FDA enforcement
Itoen (USA) INC·Food·Jun 15, 2012

Itoen Green Tea 11.5 FL OZ (340 ML) Can

What you need to know

Class II

  • What happened

    ITO EN discovered that unretorted product was inadvertently released for distribution.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDACAMore food

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Product identification

Source: FDA FOOD

Brand nameItoen (USA) INC
Recalling firmItoen (USA) INCHonolulu, HI, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • IHAPR1013
  • Costo item number 17800
  • Brown carboard tray side 1: GREEN TEA 041012 Brown cardboard side 2: GT 041013
Distribution area
CA

CA

United States

Quantity affected10 pallets - 6x 4 pks per case,
Recall initiationFDA report date: August 15, 2012
FDA recall numberF-1688-2012

Beyond the headline

The recall, in context

Itoen (USA) INC initiated this food recall on June 15, 2012. The FDA enforcement report states: ITO EN discovered that unretorted product was inadvertently released for distribution. The FDA report lists distribution as: CA.

The FDA enforcement report describes the reason as: ITO EN discovered that unretorted product was inadvertently released for distribution.

Itoen Green Tea 11.5 FL OZ (340 ML) Can was made or distributed by Itoen (USA) INC in Honolulu, HI, United States. This page reflects FDA report F-1688-2012, dated August 15, 2012.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Itoen Green Tea 11.5 FL OZ (340 ML) Can recall?

Itoen (USA) INC recalled Itoen Green Tea 11.5 FL OZ (340 ML) Can in an FDA Class II enforcement action reported as F-1688-2012. ITO EN discovered that unretorted product was inadvertently released for distribution.

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Itoen (USA) INC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1688-2012. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.