FindMyRecallSubscribe
Class I: serious health riskOngoing

Taylor Farms de Mexico S. de R.L. de C.V. Sysco Blend Lett/Rom 50/50 Noclr 4/5# Sysco Recall

SYSCO BLEND LETT/ROM 50/50 NOCLR 4/5# SYSCO BLEND LETT/ROM 70/30 NOCOLR 4/5# SYSCO BLEN…

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

Risk level
Class I
Reported by FDA
Aug 19, 2026
Recall ID
H-1290-2026
Check your lot numberHow we source this data

Summary

Taylor Farms de Mexico S. de R.L. de C.V. recalled Sysco Blend Lett/Rom 50/50 Noclr 4/5# Sysco starting Jul 17, 2026. The FDA classified it as Class I (serious health risk) and published enforcement report H-1290-2026 on Aug 19, 2026. Reason: Potential Cyclospora contamination. Status: Ongoing.

Why it was recalled

Potential Cyclospora contamination.

Product description

SYSCO BLEND LETT/ROM 50/50 NOCLR 4/5# SYSCO BLEND LETT/ROM 70/30 NOCOLR 4/5# SYSCO BLEND LETT/ROM 80/20 4/5# Iceberg, Romaine products.

Lot numbers, UPCs & expiration codes

SYSCO BLEND LETT/ROM 50/50 NOCLR 4/5# TFMX183A04 7/21/2026 TFMX191A02 7/29/2026 TFMX194B02 8/1/2026 SYSCO BLEND LETT/ROM 70/30 NOCOLR 4/5# TFMX181A02 7/19/2026 TFMX183B05 7/21/2026 TFMX185A01 7/23/2026 TFMX188A02 7/26/2026 TFMX192A01 7/30/2026 SYSCO BLEND LETT/ROM 80/20 4/5# TFMX181A02 7/19/2026 TFMX181A02 7/20/2026 TFMX182B02 7/20/2026 TFMX183A02 7/21/2026 TFMX184B03 7/22/2026 TFMX187B04 7/25/2026 TFMX188A03 7/26/2026

Where it was sold

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.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
H-1290-2026
Classification
Class I
Status
Ongoing
Recall initiated
Jul 17, 2026
FDA report date
Aug 19, 2026
Quantity
1,834 cases
Recall type
Voluntary: Firm initiated
Recalling firm
Taylor Farms de Mexico S. de R.L. de C.V.

Original FDA data

Every field from FDA enforcement report H-1290-2026, exactly as published.

Show all FDA fields
City
Doctor Mora
Status
Ongoing
Country
Mexico
Event ID
99453
Address
Carretera Dr. Mora A San Miguel De Allende Km. 16
Address (line 2)
Doctor Mora
Code information
SYSCO BLEND LETT/ROM 50/50 NOCLR 4/5# TFMX183A04 7/21/2026 TFMX191A02 7/29/2026 TFMX194B02 8/1/2026 SYSCO BLEND LETT/ROM 70/30 NOCOLR 4/5# TFMX181A02 7/19/2026 TFMX183B05 7/21/2026 TFMX185A01 7/23/2026 TFMX188A02 7/26/2026 TFMX192A01 7/30/2026 SYSCO BLEND LETT/ROM 80/20 4/5# TFMX181A02 7/19/2026 TFMX181A02 7/20/2026 TFMX182B02 7/20/2026 TFMX183A02 7/21/2026 TFMX184B03 7/22/2026 TFMX187B04 7/25/2026 TFMX188A03 7/26/2026
Report date
Aug 19, 2026
Product type
Food
Recall number
H-1290-2026
Classification
Class I
Recalling firm
Taylor Farms de Mexico S. de R.L. de C.V.
Product quantity
1,834 cases
Reason for recall
Potential Cyclospora contamination.
Voluntary / mandated
Voluntary: Firm initiated
Product description
SYSCO BLEND LETT/ROM 50/50 NOCLR 4/5# SYSCO BLEND LETT/ROM 70/30 NOCOLR 4/5# SYSCO BLEND LETT/ROM 80/20 4/5# Iceberg, Romaine products.
Distribution pattern
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.
Recall initiation date
Jul 17, 2026
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Aug 27, 2026

How we source this data

Source: U.S. Food and Drug Administration enforcement report H-1290-2026, published Aug 19, 2026. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions.

How we source and update recall data · Report incorrect information

Other recent food recalls