Pacific Coast Fruit Company Recall: Pacific Coast Fruit Company, Portland, Oregon is voluntarily recalling multiple types of bagged processed salads based on the potential contamination of Listeria monocytogenes. The firm utilized a portion of the salads that were recalled by their supplier.

🇺🇸 United States

1. October 20, 2017 - Recall initiated
2. November 8, 2017 - Reported by source
3. December 5, 2017 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0041-2018

Event ID

78343

Status

Terminated

Classification

Class I

Company

Pacific Coast Fruit Company

Product description

Carnival Cauli Florets, 6/16 oz., RETAIL item # 73633, New Seasons Market brand, UPC 10200 24467. Ingredients: Green Cauliflower, Orange Cauliflower, Purple Cauliflower, White Cauliflower.

Quantity

40 cases

Reason

Pacific Coast Fruit Company, Portland, Oregon is voluntarily recalling multiple types of bagged processed salads based on the potential contamination of Listeria monocytogenes. The firm utilized a portion of the salads that were recalled by their supplier.

Recall initiation date

October 20, 2017

Report date

November 8, 2017

Classification date

Not published in this source record

Termination date

December 5, 2017

Distribution pattern

distributed in Oregon and Washington.

UPC, lot, and code information

Best Use By Dates: 10/11/17-10/26/17.

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 78343 with 8 other product entries in Public Health Trace.

Responsible company: Pacific Coast Fruit Company

Other recalls from Pacific Coast Fruit Company

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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