Class IOngoingVoluntary: Firm initiated
GIAS FOOD INC.: food recall H-0014-2027
GIAS FOOD INC. of New York, NY recalled Lemon Alfredo Fettuccine packed in a yellow plastic sealed bag with pink and black lettering; label reads in part as… Reason: Contamination with Listeria monocytogenes. The FDA listed it as Class I in its Enforcement Report dated Oct 14, 2026; distribution: nationwide.
Record status as published: Ongoing. openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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
- Product quantity
- 1174 cases
- Reason for recall
- Contamination with Listeria monocytogenes
- Codes, lots and dates on the package
- L6081A SEP 21 2027
- Distribution pattern
- Retail locations nationwide
- Recalling firm
- GIAS FOOD INC., New York, NY
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Sep 24, 2026 |
| Classified by the FDA | Oct 6, 2026 |
| Published in the Enforcement Report | Oct 14, 2026 |
Other recalls by GIAS FOOD INC.
- H-1396-2026 · Sep 30, 2026 · Class I — Contamination with Listeria monocytogenes
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0014-2027 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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