Crab Cheese Rangoon, NET WT: 8 LB, 120 pieces of 30g / 3 Trays per master cardboard boxes, Keep Frozen, packaged in corr
Summary
The FDA issued a Class I for Crab Cheese Rangoon, NET WT: 8 LB, 120 pieces of 30g / 3 Trays per master cardbo by SE Tampa Inc dba Tampa Food. Reason: Undeclared allergens: Milk, Soy, Crustacea Shellfish, Fish.
Details
Source
Food Recall
External ID
F-0299-2025
Action Date
2024-12-25
Status
Terminated
Category
food
Product Description
Crab Cheese Rangoon, NET WT: 8 LB, 120 pieces of 30g / 3 Trays per master cardboard boxes, Keep Frozen, packaged in corrugated cardboard box.
Lot/Code Info: Lot#2411311, 2411312, 2411317, 2411318 Expiration Date: April 2025
Quantity Affected: 191 cases
Reason for Recall
Undeclared allergens: Milk, Soy, Crustacea Shellfish, Fish
Distribution
FL
Type: Voluntary: Firm initiated
Recall Initiated: 2024-11-25
Company
Tampa, FL
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 53 food recalls issued in the same week, part of 204 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 (SE Tampa Inc dba Tampa Food) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does SE Tampa Inc dba Tampa Food have FDA actions?
This is the only FDA action we have on record for SE Tampa Inc dba Tampa Food in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0299-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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