HH Fresh Trading Corp. (branded) ENOKI MUSHROOM
Recalled by HH FRESH TRADING CORP
Food recall
HH FRESH TRADING CORP
Class I — most serious
There is a reasonable chance that using this product could cause serious health problems or death.
HH FRESH TRADING CORP has recalled HH Fresh Trading Corp. (branded) ENOKI MUSHROOM, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on June 17, 2026 and was initiated on May 11, 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 HH Fresh Trading Corp. (branded) ENOKI MUSHROOM, with approximately 120 cases affected. The company behind the recall is HH FRESH TRADING CORP, based in Los Angeles, CA. The FDA describes the product as: “HH Fresh Trading Corp. (branded) ENOKI MUSHROOM; Premium Quality; Net WT/ Poids Net 150g(5.29oz) Distributed by HH Fresh Trading Exported by JIA YANG INTERNATIONAL ENTERPRISES CO., LTD. Produced by Green Farm (Taiwan) UPC: 4711498860002”
Why was HH Fresh Trading Corp. (branded) ENOKI MUSHROOM recalled?
According to the FDA, the stated reason for the recall is: “Imported Enoki Mushrooms 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 HH Fresh Trading Corp. (branded) ENOKI MUSHROOM, compare it against the product description and identifying codes (No lot codes) 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 HH FRESH TRADING CORP 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 17, 2026
- Recall started
- May 11, 2026
- Distributed in
- CA
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 HH Fresh Trading Corp. (branded) ENOKI MUSHROOM recalled?+
According to the FDA: Imported Enoki Mushrooms tested positive for Listeria Monocytogenes.
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 HH Fresh Trading Corp. (branded) ENOKI MUSHROOM?+
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.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: H-0939-2026. Information last synced from the FDA on July 6, 2026.