LEASA Industries Co., Inc. Recall: Seeds may have been contaminated with E.coli

🇺🇸 United States

1. September 4, 2026 - Recall initiated
2. October 14, 2026 - Reported by source

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

H-0003-2027

Event ID

99951

Status

Ongoing

Classification

Class I

Company

LEASA Industries Co., Inc.

Product description

LEASA Alfalfa Sprouts; packaged in plastic clamshell containers; KEEP REFRIGERATED; NET WT. 6 OZ. (170g); Grown & Packaged by: LEASA Industries Co., Inc., Mami FL 33147; Product of USA; UPC: 0 75465 11111 0

Quantity

1,416 cups

Reason

Seeds may have been contaminated with E.coli

Recall initiation date

September 4, 2026

Report date

October 14, 2026

Classification date

Not published in this source record

Termination date

Not terminated as of this source record

Distribution pattern

FL and NH

UPC, lot, and code information

Expiration Date (s): 9/4/26, 9/8/26, 9/10/26, 9/15/26, 9/17/26, 9/18/26

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

October 20, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 99951 with 1 other product entry in Public Health Trace.

Responsible company: LEASA Industries Co., Inc.

Other recalls from LEASA Industries Co., Inc.

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
Florida	1
New Hampshire	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: October 20, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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