MapleVale 18# Wet Salad Bucket Cut Cantaloupe, Honeydew, Pineapple, Grapes in Watermelon Juice with Potassium sorbat
Summary
The FDA issued a Class I for MapleVale 18# Wet Salad Bucket Cut Cantaloupe, Honeydew, Pineapple, Grapes i by Fruit Fresh Up, Inc.. Reason: may be contaminated with Listeria monocytogenes.
Details
Source
Food Recall
External ID
F-0980-2022
Action Date
2022-04-13
Status
Terminated
Category
food
Product Description
MapleVale 18# Wet Salad Bucket Cut Cantaloupe, Honeydew, Pineapple, Grapes in Watermelon Juice with Potassium sorbate added.
Lot/Code Info: BBD: 3/29/2022
Quantity Affected: 39,232 units total
Reason for Recall
may be contaminated with Listeria monocytogenes
Distribution
NY, MA, PA
Type: Voluntary: Firm initiated
Recall Initiated: 2022-03-18
Company
Depew, NY
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 31 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Fruit Fresh Up, Inc. has 12 FDA actions in our database, including 12 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 (Fruit Fresh Up, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Fruit Fresh Up, Inc. have FDA actions?
Fruit Fresh Up, Inc. has 12 FDA actions in our database, including 12 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0980-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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