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Disclaimer: Recall Radar is an informational summary of public FDA enforcement reports. It is not medical advice. Always confirm details with the FDA, the company, a pharmacist, or a doctor before making health decisions.

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Class IFood

Vitasia Asian Style Wok Spice Mix recall

Summary

Lidl US TRADING is recalling VITASIA ASIAN STYLE WOK SPICE MIX NET WT 1.58 OZ (45g) UPC 4 335619 355491 DISTR… (food). According to the FDA report, the reason is: Salmonella. The firm received a positive test result of Salmonella in the product. The FDA rated this a Class I: most serious: there is a reasonable chance the product could cause serious health problems or death. Recall status: Ongoing.

Understanding this recall

What happened

Lidl is recalling Vitasia Asian Style Wok Spice Mix after a test found Salmonella in the product.

Why it matters

Salmonella bacteria can cause salmonellosis, with diarrhea, fever and stomach cramps that usually start 6 hours to 6 days after exposure. Most people recover within a week, but young children, adults 65 and older, pregnant people and people with weakened immune systems are more likely to become seriously ill. Foods eaten raw or uncooked, like fresh peppers, salsa, sprouts and powders, can't be made safe by the consumer. Spices are often added near the end of cooking or sprinkled on food afterward, so they may not be heated enough to kill bacteria.

Who should pay attention

Lidl shoppers in DC, DE, GA, MD, NC, NJ, NY, PA, SC and VA.
Distribution in the FDA report: Washington DC, DE, GA, MD, NC, NJ, NY, PA, SC, VA.

How to check your product

Look for the lot number and best-if-used-by date on the container.
Codes listed by the FDA: Lot # 155846, Best if Used By JUN 2028

Based only on the FDA enforcement record plus general public-health background on this type of hazard. Not medical advice; if you have symptoms or concerns, contact a doctor or pharmacist.

Details from the FDA report

Product
VITASIA ASIAN STYLE WOK SPICE MIX NET WT 1.58 OZ (45g) UPC 4 335619 355491 DISTRIBUTED BY LIDL US, LLC ARLINGTON, VA 22202 PRODUCT OF THE CZECH REPUBLIC
Reason
Salmonella. The firm received a positive test result of Salmonella in the product.
Lot / code info
Lot # 155846, Best if Used By JUN 2028
Quantity
2,040 containers
Distribution
Washington DC, DE, GA, MD, NC, NJ, NY, PA, SC, VA.
Recalling company
Lidl US TRADING, Arlington, VA United States
Recall started
August 10, 2026
FDA report date
August 26, 2026
Classification
Class I: Most serious: there is a reasonable chance the product could cause serious health problems or death.
Voluntary / mandated
Voluntary: Firm initiated
Status
Ongoing
Recall number
H-1243-2026

What to do

View the FDA source record (openFDA) · FDA recalls page

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