Sirna & Sons Produce PEPPER JALAPENO BREAK 1LB, repackaged into 1 lb. plastic bags, Product Number: 55255, Packed by Sir
Summary
The FDA issued a Class I for Sirna & Sons Produce PEPPER JALAPENO BREAK 1LB, repackaged into 1 lb. plastic ba by Sirna and Sons Produce, Inc. Reason: Potential Salmonella Javiana contamination.
Details
Source
Food Recall
External ID
H-1262-2026
Action Date
2026-09-02
Status
Ongoing
Category
food
Product Description
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
Lot/Code Info: Lot Numbers: 60947409, 60991812 Pack Dates: 07/13/26, 07/23/26 Internal Product Number: 00184
Quantity Affected: 249 bags
Reason for Recall
Potential Salmonella Javiana contamination
Distribution
OH, PA (for food service use only)
Type: Voluntary: Firm initiated
Recall Initiated: 2026-08-05
Company
Ravenna, OH
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 47 food recalls issued in the same week, part of 82 food-related FDA actions this month.
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 (Sirna and Sons Produce, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Sirna and Sons Produce, Inc have FDA actions?
This is the only FDA action we have on record for Sirna and Sons Produce, Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1262-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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