FDA recall record

Gilster-Mary Lee Lightly salted microwave popcorn packaged in the following recall — FDA F-1541-2020

Popcorn ingredient was recalled due to foreign matter: tempered glass between 3 mm and 7 mm in size

Class IIclassification
F-1541-2020official record ID
Sep 30, 2020report date

Recall record at a glance

Official recordF-1541-2020
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmGilster-Mary Lee Corp.
Report dateSep 30, 2020
Recall initiation dateSep 9, 2020
QuantityCadia 320/12/3/3.3 oz/bags/boxes/cases; Lidl: 890/10/3/3.3 oz/bags/boxes/cases
LocationChester, IL, United States

Official product description

Lightly salted microwave popcorn packaged in the following ways: 1) Cadia Organic Lightly Salted Popcorn, Net Wt. 9.9 oz (281 g) 3-3.3 oz (94 g) bags, KeHDistributors LLC, Naperville, IL, UPC 15369-01288 2) Lidl, Naturally Flavored Butter Microwave Popcorn, 3-3.3 oz (94g) bags, Net Wt 9.9 oz (218 g), Distributed by LIDL US, LLC Arlington, VA UPC 40351-57962

Why the product was recalled

Popcorn ingredient was recalled due to foreign matter: tempered glass between 3 mm and 7 mm in size

Distribution information

Distributed to grocery stores in the following US States: AZ, CA, CT, FL, LA, MA, MD, MI, MN, MO, NC, NH, NY, OH, PA, TX, UT, VA, VT, WA, and WI and Canada

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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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