Herold Salads, Inc. Recall: Potential contamination with Listeria monocytogenes

🇺🇸 United States

1. December 7, 2023 - Recall initiated
2. January 24, 2024 - Reported by source
3. February 28, 2024 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0757-2024

Event ID

93644

Status

Terminated

Classification

Class I

Company

Herold Salads, Inc.

Product description

Corky's & Lenny's - Potato Salad packaged in 30lb plastic containers

Quantity

990 lbs total

Reason

Potential contamination with Listeria monocytogenes

Recall initiation date

December 7, 2023

Report date

January 24, 2024

Classification date

Not published in this source record

Termination date

February 28, 2024

Distribution pattern

Ohio, Pennsylvania, Michigan

UPC, lot, and code information

Code 12 Expiration: 12/5/2023, 12/18/2023, 12/25/2023, 1/8/2024 Lot Code: 3 10260701, 3 11080701, 3 11150701, 3 11290701

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Telephone

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 93644 with 10 other product entries in Public Health Trace.

Responsible company: Herold Salads, Inc.

Other recalls from Herold Salads, Inc.

Where this information comes from

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. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

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.

Is this recall still active?

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.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

Official guidance and record verification

Public Health Trace does not provide medical advice. The information below explains how to interpret this record and links to relevant official government sources. Review the linked official source for the current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of February 28, 2024.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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