Rucker's Wholesale & Service Co., Inc. Recall: The "Maple Nut" product label does not include peanuts as an ingredient. Peanuts are an allergen. - F-0006-2017

🇺🇸 United States

1. February 22, 2016 - Recall initiated
2. October 19, 2016 - Reported by source
3. November 2, 2018 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0006-2017

Event ID

73359

Status

Terminated

Classification

Class I

Company

Rucker's Wholesale & Service Co., Inc.

Product description

Uncle Buck's Maple Nut candy packaged in a clear plastic 2.7 oz. bag with attached green, orange, and white label with Organe and black writing.

Quantity

6,000 bags to Bass Pro Shops

Reason

The "Maple Nut" product label does not include peanuts as an ingredient. Peanuts are an allergen.

Recall initiation date

February 22, 2016

Report date

October 19, 2016

Classification date

Not published in this source record

Termination date

November 2, 2018

Distribution pattern

The products were distributed to cabela's and bass pro shops throughout the U.S. (nationwide). It was sent to 134 locations total. Including 2 consignees in Canada.

UPC, lot, and code information

Item number 7101 UPC 752545071013

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 73359 with 1 other product entry in Public Health Trace.

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 November 2, 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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