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GIAS FOOD INC. Recall: Contamination with Listeria monocytogenes

United States

OngoingClass I

Company
GIAS FOOD INC.
Product
Lemon Alfredo Fettuccine packed in a yellow plastic sealed b…
Recall date
September 3, 2026
Source
FDA

Reason for recall

Contamination with Listeria monocytogenes

  1. - Recall initiated
  2. - Reported by source
Recalled products
Product description UPC Quantity Lot / code information
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 20 2027 L6080C, UPC 194346442706, DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716 PRODUCT OF ITALY 194346442706 16,002 bags (2,286 cases) L6080C SEP 20 2027 L6079C SEP 19 2027

Distribution

  • Walmart DCs and retail locations nationwide.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
H-1396-2026
Event ID
99853
Status
Ongoing
Classification
Class I
Company
GIAS FOOD INC.
Product description
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 20 2027 L6080C, UPC 194346442706, DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716 PRODUCT OF ITALY
Quantity
16,002 bags (2,286 cases)
Reason
Contamination with Listeria monocytogenes
Recall initiation date
September 3, 2026
Report date
September 30, 2026
Classification date
Not published in this source record
Termination date
Not terminated as of this source record
Distribution pattern
Walmart DCs and retail locations nationwide.
UPC, lot, and code information
UPC 194346442706; L6080C SEP 20 2027 L6079C SEP 19 2027
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: GIAS FOOD INC.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.