VerifyRecall
Alerts
ACTIVE RECALL — CLASS IActive recallF-1760-2024/FDA enforcement
Jfe Franchising INC·Food·Jul 19, 2024

Chopped Cilantro with White Onion - 5oz Plastic Clam-shell Container

What you need to know

Class I

  • What happened

    Listeria monocytogenes

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. A hardy bacteria that can grow at refrigerator temperatures and cause severe illness in vulnerable groups.

  • 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.

Active recall · classified by the FDAKY, MI, OH, WVMore food

Advertisement

Ad

Know someone who bought this?

A quick share can keep a pantry check from becoming a missed warning.

Share via WhatsApp

Match before you discard

Product identification

Source: FDA FOOD

Brand nameJfe Franchising INC
Recalling firmJfe Franchising INCHouston, TX, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Sell by 7/9/24 THROUGH Sell by 7/26/24
Distribution area
KYMIOHWV

KY MI OH WV

United States

Quantity affectedNot provided by the FDA.
Recall initiationFDA report date: September 11, 2024
FDA recall numberF-1760-2024

Beyond the headline

The recall, in context

Jfe Franchising INC initiated this food recall on July 19, 2024. The FDA enforcement report states: Listeria monocytogenes. The FDA report lists distribution as: KY MI OH WV.

The FDA enforcement report describes the reason as: Listeria monocytogenes

Chopped Cilantro with White Onion - 5oz Plastic Clam-shell Container was made or distributed by Jfe Franchising INC in Houston, TX, United States. This page reflects FDA report F-1760-2024, dated September 11, 2024.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, a hardy bacteria that can grow at refrigerator temperatures and cause severe illness in vulnerable groups.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

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

Listeria monocytogenes

Symptoms to watch for

Fever, muscle aches, nausea and diarrhea may occur. Severe infection can cause headache, stiff neck, confusion, loss of balance or convulsions.

When symptoms may appear

Symptoms can begin within a few days, but can take up to several weeks to appear.

Higher-risk groups

Pregnant people, newborns, adults over 65 and immunocompromised people are at the highest risk of severe illness.

What to do now

  1. 1Stop using or eating the affected product and keep it away from children and pets.
  2. 2Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer.
  3. 3If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

General guidance based on CDC and FDA consumer information.

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 Chopped Cilantro with White Onion - 5oz Plastic Clam-shell Container recall?

Jfe Franchising INC recalled Chopped Cilantro with White Onion - 5oz Plastic Clam-shell Container in an FDA Class I enforcement action reported as F-1760-2024. Listeria monocytogenes

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. Stop using or eating the affected product and keep it away from children and pets. Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer. If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

Is the Jfe Franchising INC recall still active?

Yes. As of the latest FDA enforcement report, this recall is listed as ongoing. Check the official source record for the most current status before making a decision.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1760-2024. 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

More recalls by Jfe Franchising INC

View brand
Class II·

Jfe Franchising INC

" Dumpling Vegetable 4.5 OZ 011110658067 " Loaded Dumpling Vegetable 5.7 OZ 011110696953

Foreign Object (Glass)

AK, AR, AZ +34 moreFood
Class II·

Jfe Franchising INC

" Dumpling Party Tray (20pcs) Vegetable 13 OZ 011110661173 " Dumpling Party Tray (40pcs)…

Foreign Object (Glass)

AK, AR, AZ +34 moreFood

Related alerts

Recent Listeria monocytogenes recalls

All alerts
Class I·

Gias Food INC.

Lemon Alfredo Fettuccine Packed in a Yellow Plastic Sealed Bag with Pink and Black Lettering

Contamination with Listeria monocytogenes

Nationwide (US)Food
Class I·

Gias Food INC.

Lemon Alfredo Fettuccine Packed in a Yellow Plastic Sealed Bag with Pink and Black Lettering

Contamination with Listeria monocytogenes

Nationwide (US)Food

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