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RECALL RECORD — CLASS IIRecall closedF-1923-2016/FDA enforcement
Procesadora De Frutos Y Vegetales Del Caribe·Food·Jun 13, 2016

Coconut Milk, 13.5 Fld OZ, Can, 214x406 3 Pieces Steel Tins, 24 Tins Per Case

What you need to know

Class II

  • What happened

    Procesadora de Frutos y Vegetales del Caribe SRL, Calle Club Rotario 24, Madre Vieja Sur, San Crist¿bal, Dominican Republic has initiated a voluntary recall due to an…

  • 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 FDADistribution not listedMore food

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Product identification

Source: FDA FOOD

Brand nameProcesadora De Frutos Y Vegetales Del Caribe
Recalling firmProcesadora De Frutos Y Vegetales Del CaribeSan Cristobal, Dominican Republic (the)
UPC / barcodes
7 189123 23240 6
Lot / date codes
  • Lots involved are 32, 35, 37, 41, 43, 47, 39, 53 and 57. All these lots expire on May of 2018. The UPC code that identifies the P.A Coconut milk is: 7189123232406
Distribution area

U.S. consignees - New York, United States. No U.S. Government Agency consignees No Foreign consignees Please note: The firm ceased further distribution of the product(s) on 06/20/2015

United States

Quantity affected1650 cases 24/13.5fld oz
Recall initiationFDA report date: August 24, 2016
FDA recall numberF-1923-2016

Beyond the headline

The recall, in context

Procesadora De Frutos Y Vegetales Del Caribe initiated this food recall on June 13, 2016. The FDA enforcement report states: Procesadora de Frutos y Vegetales del Caribe SRL, Calle Club Rotario 24, Madre Vieja Sur, San Crist¿bal, Dominican Republic has initiated a voluntary recall due to an undeterminable number of lots of coconut milk that were thermally under processed. The FDA report lists distribution as: U.S. consignees - New York, United States. No U.S. Government Agency consignees No Foreign consignees Please note: The firm ceased further distribution of the product(s) on 06/20/2015.

The FDA enforcement report describes the reason as: Procesadora de Frutos y Vegetales del Caribe SRL, Calle Club Rotario 24, Madre Vieja Sur, San Crist¿bal, Dominican Republic has initiated a voluntary recall due to an undeterminable number of lots of coconut milk that were thermally under processed.

Coconut Milk, 13.5 Fld OZ, Can, 214x406 3 Pieces Steel Tins, 24 Tins Per Case was made or distributed by Procesadora De Frutos Y Vegetales Del Caribe in San Cristobal, Dominican Republic (the). This page reflects FDA report F-1923-2016, dated August 24, 2016.

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 UPC and lot code 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

Undeclared milk

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a milk allergy.

When symptoms may appear

Reactions can begin within minutes to a few hours after eating the product.

Higher-risk groups

People with a diagnosed cow's milk allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a milk allergy.
  2. 2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

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 Coconut Milk, 13.5 Fld OZ, Can, 214x406 3 Pieces Steel Tins, 24 Tins Per Case recall?

Procesadora De Frutos Y Vegetales Del Caribe recalled Coconut Milk, 13.5 Fld OZ, Can, 214x406 3 Pieces Steel Tins, 24 Tins Per Case in an FDA Class II enforcement action reported as F-1923-2016. Procesadora de Frutos y Vegetales del Caribe SRL, Calle Club Rotario 24, Madre Vieja Sur, San Crist¿bal, Dominican Republic has initiated a voluntary recall due to an…

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. Do not eat the product if you have a milk allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

Is the Procesadora De Frutos Y Vegetales Del Caribe 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-1923-2016. 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

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