Renaissance Food Group Recall: Firm received positive test results for L. monocytogenes in a finished product. All products manufactured with the same components are being recalled.

🇺🇸 United States

1. September 12, 2022 - Recall initiated
2. October 12, 2022 - Reported by source

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0021-2023

Event ID

90883

Status

Completed

Classification

Class I

Company

Renaissance Food Group

Product description

Seasoned Squash Onion & Dill, NET WT, 10.5 OZ (297g), Dist. By: Renaissance Food Group LLC 4322 Moreland Ave. Conley, GA 30288, UPC 8 26766 19036 2

Quantity

106/10.5 oz units

Reason

Firm received positive test results for L. monocytogenes in a finished product. All products manufactured with the same components are being recalled.

Recall initiation date

September 12, 2022

Report date

October 12, 2022

Classification date

Not published in this source record

Termination date

Not terminated as of this source record

Distribution pattern

Products were shipped to the following states: Alabama, Georgia & South Carolina.

UPC, lot, and code information

GHGA 254 SELL BY: 09/17/22

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

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 90883 with 9 other product entries in Public Health Trace.

Responsible company: Renaissance Food Group

Other recalls from Renaissance Food Group

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

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 "Completed." 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.

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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