Sheehan Brothers Vending BBQ Riblet Sandwich with Coleslaw, 8 oz (226g), in a plastic tray/2 oz cup and individually wra
Summary
The FDA issued a Class I for Sheehan Brothers Vending BBQ Riblet Sandwich with Coleslaw, 8 oz (226g), in a pl by SHEEHAN BROTHERS VENDING. Reason: Undeclared sesame.
Details
Source
Food Recall
External ID
H-0336-2025
Action Date
2025-08-06
Status
Terminated
Category
food
Product Description
Sheehan Brothers Vending BBQ Riblet Sandwich with Coleslaw, 8 oz (226g), in a plastic tray/2 oz cup and individually wrapped in plastic, UPC: 100000222744
Lot/Code Info: Prepared: Jul 1, 2025 and Sell By: Jul 7, 2025 Prepared: Jul 6, 2025 and Sell By: Jul 12, 2025
Quantity Affected: 209 individual units
Reason for Recall
Undeclared sesame
Distribution
IN, KY, OH
Type: Voluntary: Firm initiated
Recall Initiated: 2025-07-08
Company
Springfield, 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 85 food recalls issued in the same week, part of 204 food-related FDA actions this month.
SHEEHAN BROTHERS VENDING 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 (SHEEHAN BROTHERS VENDING) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does SHEEHAN BROTHERS VENDING have FDA actions?
SHEEHAN BROTHERS VENDING 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 "H-0336-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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