Wei-Chuan branded Black Fungus Slice. Net weight: 2.5 oz UPC#: 072869231321
Summary
The FDA issued a Class II for Wei-Chuan branded Black Fungus Slice. Net weight: 2.5 oz UPC#: 072869231321 by Wei-Chuan USA Inc. Reason: "Wood-Ear" mushroom tested positive for Salmonella..
Details
Source
Food Recall
External ID
H-0279-2025
Action Date
2025-07-23
Status
Terminated
Category
food
Product Description
Wei-Chuan branded Black Fungus Slice. Net weight: 2.5 oz UPC#: 072869231321
Lot/Code Info: Expiration date: 20260417; Lot: XJ17
Quantity Affected: 100 cases
Reason for Recall
"Wood-Ear" mushroom tested positive for Salmonella.
Distribution
The recalled Wei-Chuan Dried Black Fungus Slice (2.5oz / bag) were distributed in Illinois, Indiana, Iowa, Kansas, Kentucky, Michigan, Minnesota, Missouri, Nebraska, Ohio, and Wisconsin through retail stores and supermarkets.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-06-26
Company
City Of Industry, CA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 98 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (Wei-Chuan USA Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Wei-Chuan USA Inc have FDA actions?
This is the only FDA action we have on record for Wei-Chuan USA Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0279-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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