RecallHawk
Class I Recall

MARKON BLEND LETT/ROM 50/50 NOCLR 4/5# MARKON BLEND LETT/ROM 80/20 4/5# Iceberg, Romaine products.

Taylor Farms de Mexico S. de R.L. de C.V.

Summary

The FDA issued a Class I for MARKON BLEND LETT/ROM 50/50 NOCLR 4/5# MARKON BLEND LETT/ROM 80/20 4/5# Iceberg by Taylor Farms de Mexico S. de R.L. de C.V.. Reason: Potential Cyclospora contamination..

Details

Source

Food Recall

External ID

H-1289-2026

Action Date

2026-08-19

Status

Ongoing

Category

food

Product Description

MARKON BLEND LETT/ROM 50/50 NOCLR 4/5# MARKON BLEND LETT/ROM 80/20 4/5# Iceberg, Romaine products.

Lot/Code Info: MARKON BLEND LETT/ROM 50/50 NOCLR 4/5# TFMX184A03 7/19/2026 TFMX190A03 7/25/2026 TFMX191A02 7/26/2026 TFMX194B02 7/29/2026 MARKON BLEND LETT/ROM 80/20 4/5# TFMX183A02 7/21/2026 TFMX184B03 7/22/2026 TFMX185A01 7/23/2026 TFMX189B03 7/27/2026 TFMX191A03 7/29/2026

Quantity Affected: 585 cases

Reason for Recall

Potential Cyclospora contamination.

Distribution

Domestic: AL, AR, CT, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MO, MS, NC, NH, NJ, OH, OK, PA, SC, TN, TX, VA, and WI. (Subway distribution limited to: AR, LA, and TX) Foreign: Mexico.

Type: Voluntary: Firm initiated

Recall Initiated: 2026-07-17

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 63 food recalls issued in the same week, part of 82 food-related FDA actions this month.

Taylor Farms de Mexico S. de R.L. de C.V. has 21 FDA actions in our database, including 21 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Taylor Farms de Mexico S. de R.L. de C.V.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Taylor Farms de Mexico S. de R.L. de C.V. have FDA actions?

Taylor Farms de Mexico S. de R.L. de C.V. has 21 FDA actions in our database, including 21 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-1289-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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