RecallHawk
Class I Recall

AMCE GREEK SALAD AUTHENTIC FS, Refrigerated, packaged in clear plastic container, sold by pound, UPC 293070 ##### READY

Albertsons Companies LLC

Summary

The FDA issued a Class I for AMCE GREEK SALAD AUTHENTIC FS, Refrigerated, packaged in clear plastic container by Albertsons Companies LLC. Reason: Salmonella. Greek Salad products were made with recalled cucumbers from Bedner Grower's Company which are contaminated with Salmonella and implicated .

Details

Source

Food Recall

External ID

H-0010-2025

Action Date

2025-06-11

Status

Terminated

Category

food

Product Description

AMCE GREEK SALAD AUTHENTIC FS, Refrigerated, packaged in clear plastic container, sold by pound, UPC 293070 ##### READY MEALS GREEK SALAD SS, Refrigerated, packaged in clear plastic container, sold by pound, UPC 292483 ##### Star Market GREEK SALAD FS, Refrigerated, packaged in clear plastic container, sold by pound, UPC 292329 #####

Lot/Code Info: 1) SALAD GREEK AUTHENTIC FS - Sell Thru dates from May 23, 2025 to May 24, 2025 2) READY MEALS SALAD GREEK SS - Sell Thru dates from May 20, 2025 to May 24, 2025 3) SALAD GREEK FS - Sell Thru dates from May 20, 2025 to May 24, 2025

Quantity Affected: Firm did not provide

Reason for Recall

Salmonella. Greek Salad products were made with recalled cucumbers from Bedner Grower's Company which are contaminated with Salmonella and implicated in an ongoing outbreak.

Distribution

Distributed in Connecticut, Delaware, Maine, Massachusetts, Maryland, New Hampshire, New Jersey, New York, Rhode Island, Pennsylvania, Vermont, Virginia, and Washington D.C.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-05-21

Company

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 123 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-0010-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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