RecallHawk
Class I Recall

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

AH USA Group Inc

Summary

The FDA issued a Class I for Black Fungus Golden Koi 2.5 oz packages 100 bags per case UPC: 81005681145 Produ by AH USA Group Inc. Reason: Product may contain salmonella.

Details

Source

Food Recall

External ID

F-0966-2023

Action Date

2023-06-07

Status

Terminated

Category

food

Product Description

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

Lot/Code Info: BEST BEFORE OCT/2024 Lot code - TW4115

Quantity Affected: 343 cases

Reason for Recall

Product may contain salmonella

Distribution

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

Type: Voluntary: Firm initiated

Recall Initiated: 2023-05-09

Company

AH USA Group Inc

Commerce, CA

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 73 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (AH USA Group Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does AH USA Group Inc have FDA actions?

This is the only FDA action we have on record for AH USA Group Inc in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0966-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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