Amenity Box Mix Fruits and Vegetables packed in 19-20 pound cardboard box Product Code 11303
Summary
The FDA issued a Class I for Amenity Box Mix Fruits and Vegetables packed in 19-20 pound cardboard box Produc by Hardies Fruit & Vegetable Co., LP. Reason: Potential to be contaminated with Salmonella.
Details
Source
Food Recall
External ID
F-0187-2022
Action Date
2021-11-24
Status
Terminated
Category
food
Product Description
Amenity Box Mix Fruits and Vegetables packed in 19-20 pound cardboard box Product Code 11303
Lot/Code Info: Lots: X1812481 and X1815705
Quantity Affected: 4975 pounds total
Reason for Recall
Potential to be contaminated with Salmonella
Distribution
TX
Type: Voluntary: Firm initiated
Recall Initiated: 2021-10-21
Company
Dallas, TX
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 88 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Hardies Fruit & Vegetable Co., LP 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 (Hardies Fruit & Vegetable Co., LP) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Hardies Fruit & Vegetable Co., LP have FDA actions?
Hardies Fruit & Vegetable Co., LP 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-0187-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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