Shang Hao Jia, Inc food recall: Front Panel: Danshi branded Shredded Tofu
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Terminated
- Event ID
- 97145
- Recall initiated
- Jun 25, 2025
- Classified by FDA
- Jul 17, 2025
- Posted in Enforcement Report
- Jul 23, 2025
- Terminated
- Jan 13, 2026
- Recalling firm
- Shang Hao Jia, Inc
- Firm location
- Alhambra, CA, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Products in this event
- 1
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Product does not declare allergen ingredient sesame.
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Jun 25, 2025. FDA classified it 22 days later, on Jul 17, 2025. Distribution reported by FDA: 3 local (Los Angeles) grocery stores Shang Hao Jia, Inc has 2 recalls in our records.
Recalled products (1)
H-0306-2025 Class I Terminated
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
Codes / lots: Best before: 05/24/2025; Lot# 20240825001
Quantity: 50 cases (30 bags/case)
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 97145
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.