RecallRadar
High RiskReported June 10, 2026 (3 weeks ago)

Enoki Mushroom, Net Weight 150g

Recalled by IQ PRODUCE, LLC

Food recall

IQ PRODUCE, LLC

Class I — most serious

There is a reasonable chance that using this product could cause serious health problems or death.

See all recalls involving Listeria

IQ PRODUCE, LLC has recalled Enoki Mushroom, Net Weight 150g, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on June 10, 2026 and was initiated on May 14, 2026. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Enoki Mushroom, Net Weight 150g, with approximately 319 units affected. The company behind the recall is IQ PRODUCE, LLC, based in Vernon, CA. The FDA describes the product as: “Enoki Mushroom, Net Weight 150g; Product of Korea; Distributed by IQ Produce UPC: 8809316 814286”

Why was Enoki Mushroom, Net Weight 150g recalled?

According to the FDA, the stated reason for the recall is: “Imported Enoki Mushrooms samples collected by Florida Department of Health tested positive for Listeria Monocytogenes.” In plain terms, this recall relates to Listeria.

Listeria monocytogenes is a bacterium that can grow even at refrigerator temperatures, which makes it a particular concern in ready-to-eat foods. Health authorities warn that it can cause a serious infection called listeriosis, and that pregnant people, newborns, older adults, and those with weakened immune systems are especially vulnerable. This is why products potentially contaminated with Listeria are often recalled quickly.

What should you do?

If you think you may have bought Enoki Mushroom, Net Weight 150g, compare it against the product description and identifying codes (Lot UI775) before using it. This recall is currently listed as ongoing.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact IQ PRODUCE, LLC or your local health authority.

About this recall

This recall was distributed in CA. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.

Full recall details

Status
Ongoing
Date reported
June 10, 2026
Recall started
May 14, 2026
Distributed in
CA
What was recalled
Enoki Mushroom, Net Weight 150g; Product of Korea; Distributed by IQ Produce UPC: 8809316 814286
Why it was recalled (as stated by the FDA)
Imported Enoki Mushrooms samples collected by Florida Department of Health tested positive for Listeria Monocytogenes.
How to identify the affected product
Lot UI775
Amount recalled
319 units

What you can do

Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.

Quick answers

Why was Enoki Mushroom, Net Weight 150g recalled?+

According to the FDA: Imported Enoki Mushrooms samples collected by Florida Department of Health tested positive for Li…

How serious is this recall?+

Class I — most serious. There is a reasonable chance that using this product could cause serious health problems or death.

What should I do if I have Enoki Mushroom, Net Weight 150g?+

Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.

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View the official FDA record

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: H-0898-2026. Information last synced from the FDA on July 5, 2026.

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