CLASS II Food recall · Reported 21 May 2025 · FDA Enforcement Report

Beijing Soybean Paste recalled by May Flower International

May Flower International is recalling Beijing Soybean Paste, distributed in 12 states. The recall was initiated on 17 Apr 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesNo additional codes.
Quantity recalled25 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-0802-2025
FDA event ID
96717
Recalling firm
May Flower International, Maspeth, NY
Classification
Class II
Status
Terminated
Recall initiated
17 Apr 2025
FDA classified
15 May 2025
Reported
21 May 2025
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Product category
Flour

Timeline

17 Apr 2025Recall initiated by company
15 May 2025Classified by FDA+28 days
21 May 2025Published in enforcement report+6 days

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

Reason for recall

Product contains undeclared wheat.

Product as listed by the FDA

Beijing Soybean Paste, packaged in 8.82 ounce/250g red and white packages; Ingredients Soybean, Flour, Salt, Water, Potassium Sorbate; UPC: 6917799000385

Where it was distributed

AZ, CA, ID, IL, KS, KY, MO, NY, OK, TN, TX, WI

ArizonaCaliforniaIdahoIllinoisKansasKentuckyMissouriNew YorkOklahomaTennesseeTexasWisconsin

Questions about this recall

Why was it recalled?

Product contains undeclared wheat.

Which lots are affected?

No additional codes.

Where was it sold?

AZ, CA, ID, IL, KS, KY, MO, NY, OK, TN, TX, WI

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

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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