LEASA Living Alfalfa Sprouts; packaged in plastic clamshell containers; KEEP REFRIGERATED; NET WT. 4 OZ. (113g); Grown &
Summary
The FDA issued a Class I for LEASA Living Alfalfa Sprouts; packaged in plastic clamshell containers; KEEP REF by LEASA Industries Co., Inc.. Reason: Seeds may have been contaminated with E. coli.
Details
Source
Food Recall
External ID
H-0002-2027
Action Date
2026-10-14
Status
Ongoing
Category
food
Product Description
LEASA Living Alfalfa Sprouts; packaged in plastic clamshell containers; KEEP REFRIGERATED; NET WT. 4 OZ. (113g); Grown & Packaged by: LEASA Industries Co., Inc., Mami FL 33147; Product of USA; UPC: 0 75465 55912 7
Lot/Code Info: Expiration Date (s): 9/4/26, 9/8/26, 9/10/26, 9/15/26, 9/17/26, 9/18/26
Quantity Affected: 13,812 cups
Reason for Recall
Seeds may have been contaminated with E. coli
Distribution
FL and NH
Type: Voluntary: Firm initiated
Recall Initiated: 2026-09-04
Company
Miami, 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 35 food recalls issued in the same week, part of 92 food-related FDA actions this month.
LEASA Industries Co., Inc. has 2 FDA actions in our database, including 2 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 (LEASA Industries Co., Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does LEASA Industries Co., Inc. have FDA actions?
LEASA Industries Co., Inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0002-2027" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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