Gias Food Inc. food recall: Lemon Alfredo Fettuccine packed in a yellow plastic sealed bag with…
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Ongoing
- Event ID
- 100010
- Recall initiated
- Sep 24, 2026
- Classified by FDA
- Oct 6, 2026
- Posted in Enforcement Report
- Oct 14, 2026
- Recalling firm
- GIAS FOOD INC.
- Firm location
- New York, NY, 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
Contamination with Listeria monocytogenes
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 Sep 24, 2026. FDA classified it 12 days later, on Oct 6, 2026. Distribution reported by FDA: Retail locations nationwide GIAS FOOD INC. has 2 recalls in our records.
Recalled products (1)
H-0014-2027 Class I Ongoing
Lemon Alfredo Fettuccine packed in a yellow plastic sealed bag with pink and black lettering; label reads in part as "bettergoods Lemon Alfredo Fettuccine, MADE IN ITALY, NET WT 22 OZ, BEST if Used By: SEP 21 2027 L6081A, UPC 194346442706, DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716 PRODUCT OF ITALY
Codes / lots: L6081A SEP 21 2027
Quantity: 1174 cases
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 100010
- 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.