Lemon Alfredo Fettuccine packed in a yellow plastic sealed bag with pink and black lettering; label reads in part as "be
Summary
The FDA issued a Class I for Lemon Alfredo Fettuccine packed in a yellow plastic sealed bag with pink and bla by GIAS FOOD INC.. Reason: Contamination with Listeria monocytogenes.
Details
Source
Food Recall
External ID
H-0014-2027
Action Date
2026-10-14
Status
Ongoing
Category
food
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 21 2027 L6081A, UPC 194346442706, DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716 PRODUCT OF ITALY
Lot/Code Info: L6081A SEP 21 2027
Quantity Affected: 1174 cases
Reason for Recall
Contamination with Listeria monocytogenes
Distribution
Retail locations nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2026-09-24
Company
New York, NY
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 35 food recalls issued in the same week, part of 92 food-related FDA actions this month.
GIAS FOOD INC. has 2 FDA actions in our database, including 2 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 (GIAS FOOD INC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does GIAS FOOD INC. have FDA actions?
GIAS FOOD INC. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0014-2027" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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