Rucker's Wholesale & Service Co., Inc. Recall: Sunflower kernels in this product are contaminated with Listeria Monocytogenes per the original supplier, SunOpta. - F-1742-2016

🇺🇸 United States

1. June 8, 2016 - Recall initiated
2. July 27, 2016 - Reported by source
3. February 27, 2018 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1742-2016

Status

Terminated

Classification

Class I

Company

Rucker's Wholesale & Service Co., Inc.

Product description

SWEET N SALTY 7.5 OZ.packaged in a clear plastic bag with white sticky label. The product is under UPC code 052545003398 and includes the brand names Big R Store's, Coastal, and Fin feather Fur Outfitter's.

Quantity

Not published in this source record

Reason

Sunflower kernels in this product are contaminated with Listeria Monocytogenes per the original supplier, SunOpta.

Recall initiation date

June 8, 2016

Report date

July 27, 2016

Classification date

Not published in this source record

Termination date

February 27, 2018

Distribution pattern

70 retail stores nationwide. Product was also shipped to canada firms. please see attached spread sheet for a full list of customers.

UPC, lot, and code information

Not published in this source record

Voluntary or mandated

Not published in this source record

Initial notification method

Not published in this source record

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: Rucker's Wholesale & Service Co., Inc.

Other recalls from Rucker's Wholesale & Service Co., Inc.

Where this information comes from

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

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

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?

FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.

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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of February 27, 2018.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

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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