Enoki Mushroom Recall by HEMU TRADING INC

Source: FDA · United States (CA, FL, MD)

Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.

HEMU TRADING INC is recalling its Enoki Mushroom product due to potential contamination with Listeria Monocytogenes, affecting 1056 cases distributed in CA, FL, and MD.

What this FDA recall tells you, and what most readers miss

This notice was issued by FDA on May 13, 2026 and geographically references United States (CA, FL, MD). Its severity classification of "high" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.

Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to read it as a data point about the issuing system: how quickly FDA detected the hazard, how precise the geographic or product-identifier scope is, and whether similar notices have clustered in the same category or region in the last 90 days. Cluster patterns frequently precede a broader regulatory action, a single localized FDA recall is isolated; three of them within a quarter often indicate a supply-chain, infrastructure, or seasonal driver that will keep producing notices until something structural changes.

For decision-making, Areazine pairs each alert with the original agency URL, the full agency name, and a timestamp so you can verify the notice against the primary source before acting on it. Tags on this item (recall, product-safety, cpsc, Food) map to related alerts in the same area of risk - browsing them together gives a clearer picture than any single notice alone, because the shape of an ongoing issue only becomes visible across multiple sequential alerts.

What Happened

HEMU TRADING INC is recalling its Enoki Mushroom product because it tested positive for Listeria Monocytogenes.

Which Products Are Affected

The affected product is Black label with blue lettering, FOOD Korean Food, ENOKI MUSHROOM, 150g clear plastic package; Product of Korea, Keep Refrigerated, distributed by Hemu Trading Inc. It has UPC: 8801234567893, lot code: 215, and a total quantity of 1056 cases (34 packs per case). The product was distributed to 5 direct account consignees located in CA, FL, and MD.

What You Should Do

Consumers who have the product should not consume it and contact the recalling firm, HEMU TRADING INC at their address: 1400 E Olympic Blvd, Los Angeles, CA 90021-1937, as the recall was initiated voluntarily by the firm.

Why This Matters

This recall involves a Class I classification, indicating a high risk of serious health consequences from Listeria contamination. It affects food products distributed in specific U.S. states, highlighting potential food safety issues for consumers.

Source

FDA recall notice H-0686-2026

Original source: FDA Official Notice ↗

All FDA Recalls →

Frequently Asked Questions

Common questions about this FDA recall.

What is this FDA recall about?
HEMU TRADING INC is recalling its Enoki Mushroom product due to potential contamination with Listeria Monocytogenes, affecting 1056 cases distributed in CA, FL, and MD.
Which agency issued this alert?
This alert was issued by FDA. The original notice is available at the source link at the bottom of this article.
How severe is this alert?
This alert is classified as "high" severity. Take precautions and monitor for updates.
What area is affected?
This alert affects United States (CA, FL, MD). Check with FDA for the most current geographic scope.
Where can I find more FDA Recalls updates?
Browse the full FDA Recalls feed on Areazine at areazine.com/recalls/fda/ for the latest updates from FDA and other agencies.