RecallRadar
FDA · FoodClass I

Sirna and Sons Produce, Inc food recall: Sirna & Sons Produce PEPPER JALAPENO BREAK 1LB

SalmonellaMicrobial contamination

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Ongoing
Event ID
99695
Recall initiated
Aug 5, 2026
Classified by FDA
Aug 21, 2026
Posted in Enforcement Report
Sep 2, 2026
Recalling firm
Sirna and Sons Produce, Inc
Firm location
Ravenna, OH, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Products in this event
1

What to do

Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.

View the official FDA record ↗

Reason for recall

Potential Salmonella Javiana contamination

What the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on Aug 5, 2026. FDA classified it 16 days later, on Aug 21, 2026. Distribution reported by FDA: OH, PA (for food service use only)

Recalled products (1)

  • H-1262-2026 Class I Ongoing

    Sirna & Sons Produce PEPPER JALAPENO BREAK 1LB, repackaged into 1 lb. plastic bags, Product Number: 55255, Packed by Sirna & Sons Produce 7176 State Route 88, Ravenna, OH 44266, distributed for food service use only

    Codes / lots: Lot Numbers: 60947409, 60991812 Pack Dates: 07/13/26, 07/23/26 Internal Product Number: 00184

    Quantity: 249 bags

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
Official notice
FDA Enforcement Report, event 99695
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.