Werner Gourmet Meat Snacks, Inc. Recall: Jolly Rancher product is recalled due to undeclared soy lecithin.

🇺🇸 United States

1. December 4, 2019 - Recall initiated
2. December 18, 2019 - Reported by source
3. March 31, 2020 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0336-2020

Event ID

84420

Status

Terminated

Classification

Class II

Company

Werner Gourmet Meat Snacks, Inc.

Product description

Jolly Rancher product is hard candies, individually wrapped in flexible plastic wrap, and package in plastic bag. Net weight 2 oz or 4.5 oz. UPC on the 4.5 oz. bag: 7 09972 80101 0. The label of the retail bag is read in parts: INGREDIENTS: CORN SYRUP, SUGAR, CONTAINS 2% OR LESS OF, MALIC ACID, NATURAL AND ARTIFICIAL FLAVOR, ARTIFICIAL COLOR (RED 40, BLUE 3, YELLOW 5, YELLOW 6), SULFUR DIOXIDE, TO MAINTAIN FRESHNESS *** MAY CONTAIN: PEANUTS***SOY*** Product of USA *** Werner Gourmet Meat Snacks Inc. Tillamook, OR 97141 *** www.wernerjerky.com ***.

Quantity

2076 cases (12/2 oz. packages per case) and 7199 cases (6/4.5 oz. packages per case)

Reason

Jolly Rancher product is recalled due to undeclared soy lecithin.

Recall initiation date

December 4, 2019

Report date

December 18, 2019

Classification date

Not published in this source record

Termination date

March 31, 2020

Distribution pattern

distributed nationwide and in Canada.

UPC, lot, and code information

Best by: 01 NOV 2019 through Best by: 01 JAN 2021.

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: Werner Gourmet Meat Snacks, Inc.

Other recalls from Werner Gourmet Meat Snacks, 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.

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?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

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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