Jack & the Green Sprouts Alfalfa & Onion, Net Weight 5 oz (142g). UPC 7 63247-19594 5 Keep Refrigerated. Product of
Summary
The FDA issued a Class I for Jack & the Green Sprouts Alfalfa & Onion, Net Weight 5 oz (142g). UPC 7 63247- by Jack & The Green Sprouts, Inc.. Reason: Sprouts may be contaminated with Listeria monocytogenes..
Details
Source
Food Recall
External ID
F-0074-2025
Action Date
2024-11-06
Status
Completed
Category
food
Product Description
Jack & the Green Sprouts Alfalfa & Onion, Net Weight 5 oz (142g). UPC 7 63247-19594 5 Keep Refrigerated. Product of USA. Jackandthegreensprouts.com, River Falls, WI 54022
Lot/Code Info: Lot # 300. Expiration Dates 10/9/24
Quantity Affected: 1,501 units EXPANDED 10/04/2024: 9,580 units and 48 trays (total)
Reason for Recall
Sprouts may be contaminated with Listeria monocytogenes.
Distribution
IA, MN, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2024-10-01
Company
River Falls, WI
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 42 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Jack & The Green Sprouts, 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 (Jack & The Green Sprouts, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Jack & The Green Sprouts, Inc. have FDA actions?
Jack & The Green Sprouts, 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-0074-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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