FDA recall record

JML Holdings Three Way Popcorn Sampler that contains three types of popcorn recall — FDA F-0503-2017

Undeclared eggs on the finished product label.

Class Iclassification
F-0503-2017official record ID
Nov 30, 2016report date

Recall record at a glance

Official recordF-0503-2017
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmJML Holdings Inc.
Report dateNov 30, 2016
Recall initiation dateOct 21, 2016
Quantity8 cans
LocationHolland, OH, United States

Official product description

Three Way Popcorn Sampler that contains three types of popcorn (cheese, carmel and buttered popcorn) packed inside one unlabeled clear plastic bag, physically divided by a three-way paperboard divider. The bag is packed inside a metal tin.

Why the product was recalled

Undeclared eggs on the finished product label.

Distribution information

Product was distributed in the following states: IL, MI, and OH.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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