FDA recall, , High risk
Sirna & Sons Produce Jalapeño Peppers
Jalapeno peppers may be contaminated with Salmonella Javiana.
What happened
Sirna and Sons Produce, Inc., of Ravenna, Ohio, recalled 249 bags of Sirna & Sons Produce PEPPER JALAPENO BREAK 1LB, repackaged into 1 lb. plastic bags, due to potential Salmonella Javiana contamination. The product was distributed for food service use only in Ohio and Pennsylvania. The recall began on August 5, 2026, and was added to the FDA's Enforcement Report on August 21, 2026.
The jalapeno peppers were packed by Sirna & Sons Produce at 7176 State Route 88, Ravenna, OH 44266, and distributed for food service use only. The product is identified as Product Number 55255.

What to do
We don't have product-specific instructions for this recall. FDA's general advice for food recalls:
- Return it to the store where you bought it, or throw it away.
- Don't give it to anyone else, such as a food bank, or to a pet.
Is your bag affected?
Match the UPC and lot code listed under your product.
A UPC is the number printed under a barcode.
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
- UPC
- 60947409
- 60991812
- Lot code
- 00184
Recall details
- Company began the recall
- Sold in
Ohio, Pennsylvania (for food service use only)
- Company
- Sirna and Sons Produce, IncRavenna, Ohio
- Also in an FSIS alert
- Meat and Poultry products Containing FDA-Regulated Jalapeños
- Hazard
- Salmonella
- Risk
High risk
There is a reasonable chance that eating it could cause serious health problems or death.
FDA Class I recall · How risk is rated
- Event ID
- 99695
- Recall number
- H-1262-2026
- Quantity recalled
- 249 bags
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated



