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-1396-2026
Action Date
2026-09-30
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 20 2027 L6080C, UPC 194346442706, DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716 PRODUCT OF ITALY
Lot/Code Info: L6080C SEP 20 2027 L6079C SEP 19 2027
Quantity Affected: 16,002 bags (2,286 cases)
Reason for Recall
Contamination with Listeria monocytogenes
Distribution
Walmart DCs and retail locations nationwide.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-09-03
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 58 food recalls issued in the same week, part of 82 food-related FDA actions this month.
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?
This is the only FDA action we have on record for GIAS FOOD INC. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1396-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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