VITASIA ASIAN STYLE WOK SPICE MIX NET WT 1.58 OZ (45g) UPC 4 335619 355491 DISTRIBUTED BY LIDL US, LLC ARLINGTON, VA 222
Summary
The FDA issued a Class I for VITASIA ASIAN STYLE WOK SPICE MIX NET WT 1.58 OZ (45g) UPC 4 335619 355491 DISTR by Lidl US TRADING. Reason: Salmonella. The firm received a positive test result of Salmonella in the product..
Details
Source
Food Recall
External ID
H-1243-2026
Action Date
2026-08-26
Status
Ongoing
Category
food
Product Description
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
Lot/Code Info: Lot # 155846, Best if Used By JUN 2028
Quantity Affected: 2,040 containers
Reason for Recall
Salmonella. The firm received a positive test result of Salmonella in the product.
Distribution
Washington DC, DE, GA, MD, NC, NJ, NY, PA, SC, VA.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-08-10
Company
Arlington, VA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 53 food recalls issued in the same week, part of 82 food-related FDA actions this month.
Lidl US TRADING has 18 FDA actions in our database, including 18 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Lidl US TRADING) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lidl US TRADING have FDA actions?
Lidl US TRADING has 18 FDA actions in our database, including 18 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1243-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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