Beijing Soybean Paste, packaged in 8.82 ounce/250g red and white packages; Ingredients Soybean, Flour, Salt, Water, Pota
Summary
The FDA issued a Class II for Beijing Soybean Paste, packaged in 8.82 ounce/250g red and white packages; Ingre by May Flower International Inc. Reason: Product contains undeclared wheat..
Details
Source
Food Recall
External ID
F-0802-2025
Action Date
2025-05-21
Status
Terminated
Category
food
Product Description
Beijing Soybean Paste, packaged in 8.82 ounce/250g red and white packages; Ingredients Soybean, Flour, Salt, Water, Potassium Sorbate; UPC: 6917799000385
Lot/Code Info: No additional codes.
Quantity Affected: 25 cases
Reason for Recall
Product contains undeclared wheat.
Distribution
AZ, CA, ID, IL, KS, KY, MO, NY, OK, TN, TX, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2025-04-17
Company
Maspeth, NY
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 51 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 (May Flower International Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does May Flower International Inc have FDA actions?
This is the only FDA action we have on record for May Flower International Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0802-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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