(1) GINGER CHICKEN BROCCOLI SALAD FS (UPC 27110800000) (2) READY MEALS GINGER CHICKEN BROCOLLI SALAD SS (UPC 29105700000
Summary
The FDA issued a Class I for (1) GINGER CHICKEN BROCCOLI SALAD FS (UPC 27110800000) (2) READY MEALS GINGER CH by Albertsons Companies LLC. Reason: Meal kits contain cooked chicken which was recalled due to contamination with Listeria monocytogenes.
Details
Source
Food Recall
External ID
F-0248-2025
Action Date
2024-12-11
Status
Terminated
Category
food
Product Description
(1) GINGER CHICKEN BROCCOLI SALAD FS (UPC 27110800000) (2) READY MEALS GINGER CHICKEN BROCOLLI SALAD SS (UPC 29105700000) (3) GINGER BROCOLLI SALAD FS (UPC 29233600000) (4) CHICKEN CAESAR SALAD FS (UPC 29130700000) (5) CAESAR CHICKEN BOWL (UPC 29125500000) (6) READY MEALS CHICKEN CAESAR SALAD SS (UPC21139700000) (7) READY MEALS ASIAN STIR FRY SS COLC (UPC 21296500000)
Lot/Code Info: All Sell Thru dates up to and including Oct. 13, 2024
Quantity Affected: 2,374 units collectively
Reason for Recall
Meal kits contain cooked chicken which was recalled due to contamination with Listeria monocytogenes
Distribution
AK, AZ, AR, CA, ID, IL, IN, IA, LA, ME, MA, NV, NH, NM, RI, SD, TX, UT, VT, WA, & WY.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-10-10
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 107 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 "F-0248-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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