Mann Packing Company, Inc. Recall: CFIA notified FDA of positive result for Listeria monocytogenes with various best by dates of Sweet Kale Salad Blend.

🇺🇸 United States

1. November 3, 2019 - Recall initiated
2. November 27, 2019 - Reported by source
3. April 6, 2023 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0272-2020

Event ID

84190

Status

Terminated

Classification

Class II

Company

Mann Packing Company, Inc.

Product description

Marketside Cali Rice 6 x 12 oz. UPC: 681131221818 Cauli Rice - Mann 6 x 12 oz. UPC: 716519069031 6 x 12 oz. UPC: 716519067969 - Canada MNN Hungryroot: Food Kit: No UPC Cauliflower Rice 20 x 14 oz. HR Marketside: Cauli Rice 6 x 12 oz. UPC: 681131221818 Compliments - Canada UPC: 68820132547

Quantity

Total: 1,286,466 cases - US,. 141,030 cartons Canada

Reason

CFIA notified FDA of positive result for Listeria monocytogenes with various best by dates of Sweet Kale Salad Blend.

Recall initiation date

November 3, 2019

Report date

November 27, 2019

Classification date

Not published in this source record

Termination date

April 6, 2023

Distribution pattern

US and Canada and Japan

UPC, lot, and code information

UPC 681131221818; Best If Enjoyed By date of October 11, 2019 to November 16, 2019

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

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 84190 with 10 other product entries in Public Health Trace.

Responsible company: Mann Packing Company, Inc.

Other recalls from Mann Packing Company, Inc.

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 II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

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.

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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