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Policy version 2026-07-21, effective July 21, 2026.
United States
TerminatedClass I
Listeria monocytogenes. Albertson's store-made deli items contain a recalled Penne pasta ingredient which was recalled due to Listeria monocytogenes.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Smoked Mozzarella Penne Salad Kit, UPC 271876 #####. 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. | 271876 | Unknown | Sell Thru Dates: SEP 25 25 Thru OCT 4 25 |
This recall shares FDA event ID 97724 with 9 other product entries in Public Health Trace.
FDA Recall United States TerminatedTerminated: November 25, 2025Historical recordClass I
FDA Recall United States TerminatedTerminated: November 25, 2025Historical recordClass I
FDA Recall United States TerminatedTerminated: November 25, 2025Historical recordClass I
FDA Recall United States TerminatedTerminated: November 25, 2025Historical recordClass I
FDA Recall United States TerminatedTerminated: November 25, 2025Historical recordClass I
FDA Recall United States TerminatedTerminated: November 25, 2025Historical recordClass I
FDA Recall United States TerminatedTerminated: November 25, 2025Historical recordClass I
FDA Recall United States TerminatedTerminated: November 25, 2025Historical recordClass I
FDA Recall United States TerminatedTerminated: November 25, 2025Historical recordClass I
Responsible company: Albertsons Companies LLC
FDA Recall United States TerminatedTerminated: July 2, 20262026 recordClass II
FDA Recall United States TerminatedTerminated: July 2, 20262026 recordClass II
FDA Recall United States TerminatedTerminated: July 2, 20262026 recordClass II
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Alaska | 1 |
| Arkansas | 1 |
| Arizona | 1 |
| California | 1 |
| Colorado | 1 |
| Hawaii | 1 |
| Louisiana | 1 |
| Nebraska | 1 |
| New Mexico | 1 |
| Nevada | 1 |
| Oklahoma | 1 |
| South Dakota | 1 |
| Texas | 1 |
| Utah | 1 |
| Wyoming | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
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.
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
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.
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
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