RECALL RECORD — CLASS IIIRecall closedF-1133-2013/FDA enforcement

Tausi Brand Salted Black Beans

What you need to know

Class III
  • What happened

    This recall has been initiated due to suspected but, as of the writing of this letter (1/17/2013), unconfirmed Clostridium botulinum (C. botulinum) contamination.

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. Clostridium botulinum can produce a severe neurotoxin in improperly processed or stored food.

  • Action required

    Do not eat the product. Check the lot and UPC codes below, then discard it or return it to the retailer for a refund. If you have already eaten it, monitor for symptoms and seek medical care if they are severe or persistent.

Recall closed · classified by the FDAIN, NJ, NYMore food

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Product identification

Source: FDA FOOD

Brand namePhil-am Trading, INC.
Recalling firmPhil-am Trading, INC.Jersey City, NJ, United States
UPC / barcodes
8 97399 00109 7
Lot / date codes
  • UPC 897399001097
  • Best by: BB Sep 21 2010.
Distribution area
INNJNY

74 customers mainly located in NJ, NY and Pennsylvania.

United States

Quantity affected247 Cartons (100 cans per carton).
Recall initiationFDA report date: March 20, 2013
FDA recall numberF-1133-2013

Beyond the headline

The recall, in context

Phil-am Trading, INC. initiated this food recall on January 18, 2013. The FDA enforcement report states: This recall has been initiated due to suspected but, as of the writing of this letter (1/17/2013), unconfirmed Clostridium botulinum (C. botulinum) contamination. The FDA report lists distribution as: 74 customers mainly located in NJ, NY and Pennsylvania.

The FDA enforcement report describes the reason as: This recall has been initiated due to suspected but, as of the writing of this letter (1/17/2013), unconfirmed Clostridium botulinum (C. botulinum) contamination.

Tausi Brand Salted Black Beans was made or distributed by Phil-am Trading, INC. in Jersey City, NJ, United States. This page reflects FDA report F-1133-2013, dated March 20, 2013.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, clostridium botulinum can produce a severe neurotoxin in improperly processed or stored food.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

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

Botulism

Symptoms to watch for

Possible blurred or double vision, drooping eyelids, slurred speech, difficulty swallowing, muscle weakness and breathing difficulty. Seek urgent medical care for these symptoms.

When symptoms may appear

Neurological symptoms typically begin 12 to 36 hours after exposure, but can appear sooner or later.

Higher-risk groups

Infants, older adults, pregnant people and people with weakened immune systems are especially vulnerable.

What to do now

  1. 1Do not taste, eat or use the affected product, even if it looks or smells normal.
  2. 2Seek urgent medical care immediately if anyone has neurological or breathing symptoms; do not wait for test results.
  3. 3Keep the product packaging and contact the recalling firm or retailer about a refund or safe disposal.

Botulism is a medical emergency. Contact emergency services for breathing or neurological symptoms.

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 Tausi Brand Salted Black Beans recall?

Phil-am Trading, INC. recalled Tausi Brand Salted Black Beans in an FDA Class III enforcement action reported as F-1133-2013. This recall has been initiated due to suspected but, as of the writing of this letter (1/17/2013), unconfirmed Clostridium botulinum (C. botulinum) contamination.

What are the symptoms of Botulism exposure?

Possible blurred or double vision, drooping eyelids, slurred speech, difficulty swallowing, muscle weakness and breathing difficulty. Seek urgent medical care for these symptoms.

How quickly can Botulism symptoms appear?

Neurological symptoms typically begin 12 to 36 hours after exposure, but can appear sooner or later.

Who is most at risk from Botulism?

Infants, older adults, pregnant people and people with weakened immune systems are especially vulnerable.

What should I do if I bought this product?

Do not eat the product. Check the lot and UPC codes below, then discard it or return it to the retailer for a refund. If you have already eaten it, monitor for symptoms and seek medical care if they are severe or persistent. Do not taste, eat or use the affected product, even if it looks or smells normal. Seek urgent medical care immediately if anyone has neurological or breathing symptoms; do not wait for test results. Keep the product packaging and contact the recalling firm or retailer about a refund or safe disposal.

How do I get a refund from Phil-am Trading, INC.?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-1133-2013 and keep the packaging, lot code and proof of purchase if you have them.

Is the Phil-am Trading, 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-1133-2013. 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.