CLASS I Food recall · Reported 23 Jul 2025 · FDA Enforcement Report

Front Panel: Danshi branded Shredded Tofu Rear Panel recalled

Shang Hao Jia is recalling Front Panel: Danshi branded Shredded Tofu Rear Panel: Best before: 05/24/2025. The recall was initiated on 25 Jun 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBest before: 05/24/2025; Lot# 20240825001
Quantity recalled50 cases (30 bags/case)

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
H-0306-2025
FDA event ID
97145
Recalling firm
Shang Hao Jia, Alhambra, CA
Classification
Class I
Status
Terminated
Recall initiated
25 Jun 2025
FDA classified
17 Jul 2025
Reported
23 Jul 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Sesame
Product category
Plant-Based Meat

Timeline

25 Jun 2025Recall initiated by company
17 Jul 2025Classified by FDA+22 days
23 Jul 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 does not declare allergen ingredient sesame.

Product as listed by the FDA

Front Panel: Danshi branded Shredded Tofu, 200g Rear Panel: Best before: 05/24/2025, Imported by: Shang Hao Jia, Inc. Address: South El Monte, CA 91733. Product of China. Manufacturer: Sichuan Shifang Danshi Food Co., Ltd. UPC: 6 942849 709499

Where it was distributed

3 local (Los Angeles) grocery stores

Questions about this recall

Why was it recalled?

Product does not declare allergen ingredient sesame.

Which lots are affected?

Best before: 05/24/2025; Lot# 20240825001

Where was it sold?

3 local (Los Angeles) grocery stores

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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