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CriticalFDAfda-H-0184-2025SALMONELLA CONTAMINATION

ZENSHI HANDCRAFTED SUSHI Spicy California Roll 10pc Net Wt. 7.4oz UPC 0 23012 94404 9 & UPC 0 23012 95146 7

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (Salmonella contamination). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
30,174
Recall Date
May 20, 2025
Issuing Agency
Hazard
Salmonella Contamination

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-H-0184-2025.

Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-H-0184-2025.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Harris Teeter or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-H-0184-2025.

Harris Teeter

FDA

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The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

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Harris Teeter Recall FAQ

Harris Teeter is the subject of a food safety report: ZENSHI HANDCRAFTED SUSHI Spicy California Roll 10pc Net Wt. 7.4oz UPC 0 23012 94404 9 & UPC 0 23012 95146 7. The notice was published on May 20, 2025 by the U.S. Food and Drug Administration (FDA). Approximately 30,174 units are potentially affected.