Food Recall Check
Class I · High risk Terminated Initiated May 25, 2021 (5 years ago)

Organic Microwave Butter Popcorn in cartons labeled to be Organic Microwave Popcorn Salted recall

Recalled by Gilster-Mary Lee Corp. · Chester, IL, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Butter microwave popcorn bags were packaged in organic salted popcorn consumer boxes and therefore contain undeclared milk

Undeclared allergen: Milk

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Organic Microwave Butter Popcorn in cartons labeled to be Organic Microwave Popcorn Salted, Net Wt 8.7 OZ, Distributed by TOPCO Associates LLC Elk Grove, IL, UPC 0 36800 40611 7

Quantity: 413 cases

Food: Milk & dairy Chips & snacks

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Best By APR 09 22, Lot APR0922N2

Where it was sold

Arizona California Connecticut Michigan Minnesota New Hampshire New York Pennsylvania Utah

FDA's distribution note: Distributed to distribution centers in AZ, CA, CT, MI, MN, NH, NY, PA and UT

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to milk; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Gilster-Mary Lee Corp.
Initiated by
Voluntary: Firm initiated
Recall initiated
May 25, 2021
In FDA report of
Jun 16, 2021
Terminated
Jul 19, 2021
FDA recall number
F-0659-2021 · event 87997
Official record
FDA enforcement report search

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