Meijer Inc./Traffic Dept. Recall: potential risk of Salmonella

🇺🇸 United States

1. October 5, 2020 - Recall initiated
2. November 18, 2020 - Reported by source
3. November 12, 2020 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0097-2021

Event ID

86561

Status

Terminated

Classification

Class I

Company

Meijer Inc./Traffic Dept.

Product description

FRESH FROM MEIJER CANTALOUPE CHUNKS LARGE BOWL, 32oz Clear plastic container, UPC 219323109721. FRESH FROM MEIJER CANTALOUPE CHUNKS SMALL BOWL, 16oz Clear plastic container, UPC 220196109725. FRESH FROM MEIJER CANTALOUPE CHUNKS KOSHER - LG, 32oz Clear plastic container, UPC 220616800089 FRESH FROM MEIJER CANTALOUPE CHUNKS KOSHER - SM, 16oz Clear plastic container, UPC 220617801030

Quantity

47246 units

Reason

potential risk of Salmonella

Recall initiation date

October 5, 2020

Report date

November 18, 2020

Classification date

Not published in this source record

Termination date

November 12, 2020

Distribution pattern

Meijer stores in Michigan, Ohio, Indiana, Illinois, Kentucky and Wisconsin.

UPC, lot, and code information

UPC 219323109721; sold between Sept. 26 and Oct. 5 Oldest Best By date 10/8/2020

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 86561 with 10 other product entries in Public Health Trace.

Responsible company: Meijer Inc./Traffic Dept.

Other recalls from Meijer Inc./Traffic Dept.

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 "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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