Snyder's-Lance Inc. Recall: Snyder's Lance is voluntarily recalling 6.5 oz. Emerald brand walnuts due to the presence of undeclared peanuts, almonds, cashews, and pecans. - F-0884-2018

🇺🇸 United States

1. February 21, 2018 - Recall initiated
2. March 14, 2018 - Reported by source

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0884-2018

Event ID

79311

Status

Ongoing

Classification

Class II

Company

Snyder's-Lance Inc.

Product description

Emerald brand Glazed Walnuts; Net WT. 6.5 OZ; Re-sealable pouch

Quantity

60 cases

Reason

Snyder's Lance is voluntarily recalling 6.5 oz. Emerald brand walnuts due to the presence of undeclared peanuts, almonds, cashews, and pecans.

Recall initiation date

February 21, 2018

Report date

March 14, 2018

Classification date

Not published in this source record

Termination date

Not terminated as of this source record

Distribution pattern

U.S. - Nationwide

UPC, lot, and code information

Best Before DEC 15 2018; Lot Code: EN1216XX2; Package UPC: 010300808947; Case UPC: 010300930648;

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

Responsible company: Snyder's-Lance Inc.

Other recalls from Snyder's-Lance 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 II mean?

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

Is this recall still active?

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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

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Compare the product name, brand, package size, UPC, lot code, and date information on your product with the official record to see whether it matches.

This is FDA's general Enforcement Report entry for this product -- Public Health Trace has not linked a separate FDA consumer announcement to this record.

Public Health Trace last retrieved this record on July 18, 2026.

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View the official FDA record · General recall guidance from FDA

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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