CLASS I Food recall · Reported 7 Jun 2023 · FDA Enforcement Report

Black Fungus Golden Koi packages recalled by AH USA Group

AH USA Group is recalling Black Fungus Golden Koi packages, distributed in 19 states. The recall was initiated on 9 May 2023 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBEST BEFORE OCT/2024 Lot code - TW4115
Quantity recalled343 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0966-2023
FDA event ID
92332
Recalling firm
AH USA Group, Commerce, CA
Classification
Class I
Status
Terminated
Recall initiated
9 May 2023
FDA classified
31 May 2023
Reported
7 Jun 2023
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Salmonella
Product category
Other

Timeline

9 May 2023Recall initiated by company
31 May 2023Classified by FDA+22 days
7 Jun 2023Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product may contain salmonella

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

Black Fungus Golden Koi 2.5 oz packages 100 bags per case UPC: 81005681145 Product of China

Where it was distributed

Product distributed in PA, CA, FL, MN, WI, OH, TX, TN, NM, GA, LA, KS, AK, NV, AZ, NE, IN, CO, and OK.

AlaskaArizonaCaliforniaColoradoFloridaGeorgiaIndianaKansasLouisianaMinnesotaNebraskaNew MexicoNevadaOhioOklahomaPennsylvaniaTennesseeTexasWisconsin

Questions about this recall

Why was it recalled?

Product may contain salmonella

Which lots are affected?

BEST BEFORE OCT/2024 Lot code - TW4115

Where was it sold?

Product distributed in PA, CA, FL, MN, WI, OH, TX, TN, NM, GA, LA, KS, AK, NV, AZ, NE, IN, CO, and OK.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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