FDA recall record

Albertsons Companies UPC 29120700000 Ready Meals SALAD SMOKED SALMON & FETA PASTA recall — FDA H-1059-2026

Contains statement does not declare Salmon

Class IIIclassification
H-1059-2026official record ID
Jun 10, 2026report date

Recall record at a glance

Official recordH-1059-2026
CategoryFood Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmAlbertsons Companies LLC
Report dateJun 10, 2026
Recall initiation dateMay 6, 2026
Quantity34 units
LocationBoise, ID, United States

Official product description

UPC 29120700000 Ready Meals SALAD SMOKED SALMON & FETA PASTA SS UPC 29137800000 SALAD SMOKED SALMON & FETA PASTA FS COLD This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.

Why the product was recalled

Contains statement does not declare Salmon

Distribution information

Nationwide.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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