Poblano packaged as 5lb half sliced with 2 bags per case, 5lb fourth diced with 2 bags per case, 5lb half diced with 2 b
Summary
The FDA issued a Class I for Poblano packaged as 5lb half sliced with 2 bags per case, 5lb fourth diced with by RS Hanline and Company Inc. Reason: Potential contamination with Listeria monocyotgenes.
Details
Source
Food Recall
External ID
F-1711-2024
Action Date
2024-08-21
Status
Terminated
Category
food
Product Description
Poblano packaged as 5lb half sliced with 2 bags per case, 5lb fourth diced with 2 bags per case, 5lb half diced with 2 bags per case
Lot/Code Info: Sliced Poblano 27551 Diced Poblano 27551
Quantity Affected: 16 cases
Reason for Recall
Potential contamination with Listeria monocyotgenes
Distribution
Kentucky, New York, Ohio, Pennsylvania, West Virginia, Virginia, North Carolina, Illinois, Michigan
Type: Voluntary: Firm initiated
Recall Initiated: 2024-07-19
Company
Shelby, 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 125 food recalls issued in the same week, part of 204 food-related FDA actions this month.
RS Hanline and Company Inc has 6 FDA actions in our database, including 6 recalls.
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 (RS Hanline and Company Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does RS Hanline and Company Inc have FDA actions?
RS Hanline and Company Inc has 6 FDA actions in our database, including 6 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1711-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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