FDAClass I · Food · Recall H-0939-2026 · Recalled June 17, 2026

HH Fresh Trading Corp recall — HH FRESH TRADING CORP

Agency report date: June 17, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named: HH Fresh Trading Corp
Company / brand: HH FRESH TRADING
Lot / serial / date codes: No lot codes
Distribution: Product was distributed to a single customer located in Texas. Product was further distributed as samples were collected in Florida.

Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Imported Enoki Mushrooms tested positive for Listeria Monocytogenes.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class I: most serious — reasonable probability of serious health consequences or death.

Affected product: HH Fresh Trading Corp

3. Open the official notice or contact

View the official FDA enforcement record (openFDA) ↗

Official recall ID: H-0939-2026
Brand: HH FRESH TRADING
Classification: Class I
Units affected: 120 cases
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Affected products

HH Fresh Trading Corp

Companies & origin

Recalling firm location: Los Angeles, CA, United States
Firm address: 3839 Dozier St, N/A, 90063-1827

Identifying details (verbatim from the notice)

Product codes / lots: No lot codes
Distribution: Product was distributed to a single customer located in Texas. Product was further distributed as samples were collected in Florida.
Firm notified the public via: Telephone
FDA event ID: 98993
Recall initiated: May 11, 2026
FDA classified: June 10, 2026
FDA report date: June 17, 2026

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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