Ultra Tuna Salad Cup, brand DishD'Lish, packaged in plastic cup. Label declares Housemade Albacore Tuna Salad, Arugula
Summary
The FDA issued a Class I for Ultra Tuna Salad Cup, brand DishD'Lish, packaged in plastic cup. Label declare by Hms Host International Inc. Reason: Ultra Tuna Salad in a Cup label does not declare egg..
Details
Source
Food Recall
External ID
F-0931-2023
Action Date
2023-05-31
Status
Terminated
Category
food
Product Description
Ultra Tuna Salad Cup, brand DishD'Lish, packaged in plastic cup. Label declares Housemade Albacore Tuna Salad, Arugula, Cucumber and Cherry Tomatoes.
Lot/Code Info: Expiration date: 5/3/23.
Quantity Affected: 19 cups
Reason for Recall
Ultra Tuna Salad in a Cup label does not declare egg.
Distribution
distributed in WA.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-05-03
Company
Bethesda, MD
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 71 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Hms Host International Inc has 3 FDA actions in our database, including 3 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 (Hms Host International Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Hms Host International Inc have FDA actions?
Hms Host International Inc has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0931-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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