Ready Meals Smoked Mozzarella Penne Pasta Salad, UPC 291298 #####. Product was made in-store with store generated scale
Summary
The FDA issued a Class I for Ready Meals Smoked Mozzarella Penne Pasta Salad, UPC 291298 #####. Product was m by Albertsons Companies LLC. Reason: Listeria monocytogenes. Albertson's store-made deli items contain a recalled Penne pasta ingredient which was recalled due to Listeria monocytogenes..
Details
Source
Food Recall
External ID
H-0126-2026
Action Date
2025-10-29
Status
Terminated
Category
food
Product Description
Ready Meals Smoked Mozzarella Penne Pasta Salad, UPC 291298 #####. Product was made in-store with store generated scale label applied to the container. Sold under store banners Carrs-Safeway, Eagle, and Safeway in AK.
Lot/Code Info: Sell Thru Dates: SEP 25 25 Thru OCT 4 25
Quantity Affected: Unknown
Reason for Recall
Listeria monocytogenes. Albertson's store-made deli items contain a recalled Penne pasta ingredient which was recalled due to Listeria monocytogenes.
Distribution
Distributed in AK, AR, AZ, CA, CO, HI, LA, NE, NM, NV, OK, SD, TX, UT, and WY.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-09-26
Company
Boise, ID
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 91 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Albertsons Companies LLC has 174 FDA actions in our database, including 174 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 (Albertsons Companies LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Albertsons Companies LLC have FDA actions?
Albertsons Companies LLC has 174 FDA actions in our database, including 174 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0126-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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