FDA recall H-1279-2026 · Aug 19, 2026
Taylor Farms de Mexico S. de R.L. de C.V.: Cross Valley Farms LETTUCE CHOP 4/5# Cross Valley Farms LETTUCE SHRED 1/4" 4/5# Cross Vall recall
Product
Cross Valley Farms LETTUCE CHOP 4/5# Cross Valley Farms LETTUCE SHRED 1/4" 4/5# Cross Valley Farms LETTUCE SHRED 1/8" 4/5# Iceberg only products.
Reason for recall
Potential Cyclospora contamination.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your package, and look for the company's notice on FDA's recalls page. If you have the product and aren't sure, don't use it until you've checked.
Recall details
- FDA classification
- Class I: FDA's most serious class, where use of or exposure to the product may cause serious health problems or death.
- Status
- Ongoing
- Codes, lots and dates
- Cross Valley Farms LETTUCE CHOP 4/5# TFMX183A04 7/20/2026 TFMX184A03 7/21/2026 TFMX188A02 7/25/2026 TFMX190A02 7/27/2026 TFMX195B04 8/1/2026 Cross Valley Farms LETTUCE SHRED 1/4" 4/5# TFMX182A04 7/19/2026 TFMX183A01 7/20/2026 TFMX184B01 7/21/2026 TFMX185A04 7/22/2026 TFMX187B03 7/24/2026 TFMX188A04 7/25/2026 TFMX190A04 7/27/2026 TFMX190B01 7/27/2026 TFMX191A04 7/28/2026 TFMX194B03 7/31/2026 TFMX196A02 8/2/2026 Cross Valley Farms LETTUCE SHRED 1/8" 4/5# TFMX183A04 7/20/2026 TFMX184A04 7/21/2026 TFMX185A01 7/22/2026 TFMX187B03 7/24/2026 TFMX188A04 7/25/2026 TFMX189A03 7/26/2026 TFMX190A03 7/27/2026 TFMX190A04 7/27/2026 TFMX191A04 7/28/2026 TFMX191B04 7/28/2026 TFMX192A01 7/29/2026 TFMX192A02 7/29/2026 TFMX195A04 8/1/2026 TFMX195B03 8/1/2026 TFMX196B02 8/2/2026
- Quantity
- 10,384 cases
- 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.
- Recalling firm
- Taylor Farms de Mexico S. de R.L. de C.V., Doctor Mora
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-07-17
Source: openFDA enforcement record H-1279-2026 · search recall number H-1279-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 14, 2026, 1:15 AM EDT. The agency notice is the final word.
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