Class IITerminated in FDA datasetRecall initiated Dec 4, 2019

Jolly Rancher product is hard candies, individually wrapped in flexible plastic wrap, and…

Recalling firm: Werner Gourmet Meat Snacks, Inc.

Why it was recalled

Jolly Rancher product is recalled due to undeclared soy lecithin.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 31, 2020.

Check your package

Compare the exact product and package details with the label you have.

ProductJolly 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 ***.
Package size2 oz

FDA code information

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

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original 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 ***.

Original FDA recall reason

Jolly Rancher product is recalled due to undeclared soy lecithin.

Recall details

Recall number
F-0336-2020
Event ID
84420
FDA status
Terminated
Initiated
Dec 4, 2019
Reported
Dec 18, 2019
Classified
Dec 12, 2019
Terminated
Mar 31, 2020
Quantity
2076 cases (12/2 oz. packages per case) and 7199 cases (6/4.5 oz. packages per case)
Location
Tillamook, OR, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

distributed nationwide and in Canada.

FDA source record · F-0336-2020

Data updated September 16, 2026. View official FDA data ↗

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