RecallRadar
FDA · FoodClass I

Lidl US TRADING food recall: Vitasia Asian Style Wok Spice Mix Net Wt 1.58 Oz

Salmonella

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Ongoing
Event ID
99618
Recall initiated
Aug 10, 2026
Classified by FDA
Aug 18, 2026
Posted in Enforcement Report
Aug 26, 2026
Recalling firm
Lidl US TRADING
Firm location
Arlington, VA, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Other
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.

View the official FDA record ↗

Reason for recall

Salmonella. The firm received a positive test result of Salmonella in the product.

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 Aug 10, 2026. FDA classified it 8 days later, on Aug 18, 2026. Distribution reported by FDA: Washington DC, DE, GA, MD, NC, NJ, NY, PA, SC, VA. Lidl US TRADING has 16 recalls in our records.

Recalled products (1)

  • H-1243-2026 Class I Ongoing

    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

    Codes / lots: Lot # 155846, Best if Used By JUN 2028

    Quantity: 2,040 containers

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 99618
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.