Summary
The FDA issued a Class I for READY MEALS TUNA SALAD SNACKER TRAY by Albertsons Companies LLC. Reason: Potential contamination with Listeria monocytogenes..
Details
Source
Food Recall
External ID
H-0479-2025
Action Date
2025-08-20
Status
Terminated
Category
food
Product Description
READY MEALS TUNA SALAD SNACKER TRAY
Lot/Code Info: Jul 17 25; Jul 18 25; Jul 19 25; Jul 24 25; Jul 25 25; Jul 26 25; Jul 27 25; Jul 28 25; Jul 29 25; UPC: 21151300000
Quantity Affected: Unknown
Reason for Recall
Potential contamination with Listeria monocytogenes.
Distribution
Jewel Osco products sold in IA, IL, and IN. Albertsons, Randalls, and Tom Thumb products distributed in AR, LA, OK, and TX.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-07-17
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 113 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-0479-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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