FDA recall record

Preferred Popcorn Organic Yellow Popcorn packaged in the following ways: 1) recall — FDA F-1437-2020

Popcorn may contain foreign material: tempered glass between 3 mm and 7 mm in size

Class IIclassification
F-1437-2020official record ID
Sep 16, 2020report date

Recall record at a glance

Official recordF-1437-2020
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmPreferred Popcorn
Report dateSep 16, 2020
Recall initiation dateAug 28, 2020
Quantity1,162,117 lbs
LocationChapman, NE, United States

Official product description

Organic Yellow Popcorn packaged in the following ways: 1) Great Northern Organic Popcorn, Net Wt. 5 Pounds (2.26 Kilograms), UPC 6 10708 14709 1; 2) Hometown Food Company, Organic Butterfly Popcorn, 2200 LBS, Preferred Popcorn LLC Chapman, NE; 3) Lesser Evil, Organic Yellow Butterfly Popcorn, 2185 LBS Preferred Popcorn LLC Chapman, NE; 4) Medium Organic Yellow Popcorn, 25 LB (11.34 Kg) Preferred Popcorn LLC; 5) Medium Organic Yellow Popcorn, 50 LB (22.68 Kg) Preferred Popcorn LLC; 6) Shearer's, Organic Yellow Butterfly Popcorn, 2200 LBS, Preferred Popcorn LLC Chapman, NE; 7) Specialty Food Group, Organic Yellow Butterfly Popcorn, 2200 LBS, Preferred Popcorn LLC Chapman, NE; 8) Trader Joes Organic Popping Corn, Net Wt. 28 OZ (1 lb 12 oz) 794 g, Dist. & Sold Exclusively by Trader Joe's Monrovia, CA UPC 0094 5288 9) Troystar Packaging, Inc. Organic Butterfly Popcorn, 2000 LBS, Preferred Popcorn LLC Chapman, NE; 10) Whole Alternatives, Organic Butterfly Popcorn, 2000 LBS, Preferred Popcorn LLC Chapman, NE; 11) Preferred Popcorn Organic Yellow Popcorn, Net Wt. 28oz / 794 g, Preferred Popcorn, LLC, Chapman, NE, UPC 7 64256 44035 4 12) Preferred Popcorn Organic Butterfly Popcorn, Net Wt. 50 lbs (22.68 kg), Preferred Popcorn, LLC, Chapman, NE, UPC 7 64256 30002 3

Why the product was recalled

Popcorn may contain foreign material: tempered glass between 3 mm and 7 mm in size

Distribution information

Distributed to the US States CA, CO, CT, FL, IA, IL, KY, OH, SD, WI, and British Columbia, 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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