United Natural Trading Inc. dba Woodstock Farms Recall: The firm's supplier (of dates/apricots) found Listeria monocytogenes within their facility. As a safety precaution, the firm has recalled their products that may contain dates/apricots.

🇺🇸 United States

1. June 15, 2017 - Recall initiated
2. August 9, 2017 - Reported by source
3. January 31, 2018 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-3344-2017

Event ID

77663

Status

Terminated

Classification

Class I

Company

United Natural Trading Inc. dba Woodstock Farms

Product description

Market Basket Cascade Trail Mix 11oz.

Quantity

71 Cases

Reason

The firm's supplier (of dates/apricots) found Listeria monocytogenes within their facility. As a safety precaution, the firm has recalled their products that may contain dates/apricots.

Recall initiation date

June 15, 2017

Report date

August 9, 2017

Classification date

Not published in this source record

Termination date

January 31, 2018

Distribution pattern

The products were shipped to retailers and distributors in limited quantities throughout the United States.

UPC, lot, and code information

Lot # 17156, UPC # 049705408377

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 77663 with 8 other product entries in Public Health Trace.

Responsible company: United Natural Trading Inc. dba Woodstock Farms

Other recalls from United Natural Trading Inc. dba Woodstock Farms

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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