Recall record at a glance
| Official record | F-1544-2020 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Gilster-Mary Lee Corp. |
| Report date | Sep 30, 2020 |
| Recall initiation date | Sep 9, 2020 |
| Quantity | FC: 1,890/12/3/2.9 oz/bags/boxes/cases; Sprouts: 401/12/3/2.9 oz/bags/boxes/cases; Lifesmart: 71/12/3/82 g/bags/boxes/cases; NP: 4,721 cases |
| Location | Chester, IL, United States |
Official product description
Microwave popcorn packaged in the following ways: 1) Full Circle Organic Microwave Popcorn Salted, 3-2.9 oz (82 g) bags, Net Wt. 8.7 oz (247 g), Distributed by Topco Associates LLC, Elk Grove Villiage, IL, UPC 36800-40611 2) Sprouts Farmers Market, Organic Salted Microwave Popcorn, 3-2.9 oz (82 g) bags, Net Wt. 8.7 oz (247 g), Manufactured Exclusively For Sprouts Farmers Market Phoenix AZ UPC 46670-31918 3) Life Smart Organic Microwave Popping Corn Original, 3 bags x 82 g 246 g, Imported For Metro Brands Montreal Quebec, UPC 59749-97320; 4) Nature's Promise, Organic Microwave Popcorn Slightly Salted, 3-2.9 oz (82 g) bags, Net Wt. 8.7 oz (247 g), Distributed by Foodhold USA, LLC Landover, MD UPC 88267-05575
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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