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
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 2023 | Recall initiated by company | |
| 31 May 2023 | Classified by FDA | +22 days |
| 7 Jun 2023 | Published 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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