Cross Valley Farms BLEND LETT/ROM 50/50 NOCLR 4/5# Cross Valley Farms BLEND LETT/ROM 80/20 4/5# Iceberg, Romaine product
Summary
The FDA issued a Class I for Cross Valley Farms BLEND LETT/ROM 50/50 NOCLR 4/5# Cross Valley Farms BLEND LETT by Taylor Farms de Mexico S. de R.L. de C.V.. Reason: Potential Cyclospora contamination..
Details
Source
Food Recall
External ID
H-1288-2026
Action Date
2026-08-19
Status
Ongoing
Category
food
Product Description
Cross Valley Farms BLEND LETT/ROM 50/50 NOCLR 4/5# Cross Valley Farms BLEND LETT/ROM 80/20 4/5# Iceberg, Romaine products.
Lot/Code Info: Cross Valley Farms BLEND LETT/ROM 50/50 NOCLR 4/5# TFMX183A05 7/20/2026 TFMX183B05 7/20/2026 TFMX184A03 7/21/2026 TFMX188A02 7/25/2026 TFMX189A03 7/26/2026 TFMX190B02 7/27/2026 TFMX191A02 7/28/2026 TFMX194B02 7/31/2026 TFMX195B04 8/1/2026 Cross Valley Farms BLEND LETT/ROM 80/20 4/5# TFMX184B03 7/21/2026 TFMX185A01 7/22/2026 TFMX187B04 7/24/2026 TFMX188B02 7/25/2026 TFMX191A03 7/28/2026 TFMX194B02 7/31/2026 TFMX196A02 8/2/2026
Quantity Affected: 1,956 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
Company
Doctor Mora
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-1288-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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