Severity
Moderate
FDA Food recall · Reported September 30, 2020
Popcorn ingredient was recalled due to foreign matter: tempered glass between 3 mm and 7 mm in size
The recall
Gilster-Mary Lee Corp. issued this moderate-severity FDA Food recall — Popcorn ingredient was recalled due to foreign matter: tempered glass between 3 mm and 7 mm in size.
Sourced from official FDA Food enforcement records. Verify recall #F-1543-2020 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-1543-2020) was formally reported on September 30, 2020, with the manufacturer initiating the action on September 9, 2020. It is classified under Moderate severity (Class II), with a current status of Terminated. Gilster-Mary Lee Corp. is listed as the recalling firm, operating out of Chester, IL. Federal records list the affected scope as Full Circle: 2,742/12/3/3.3 oz/bags/boxes/cases; Sprouts: 371/12/3/3.3 oz/bags/boxes/cases; Lifesmart: 336/12/3/94 g/bags/boxes/cases.
The documented reason for this recall is: Popcorn ingredient was recalled due to foreign matter: tempered glass between 3 mm and 7 mm in size Distribution data in the federal record shows the product reached: 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. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Food — clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category — 319 appliances recalls on record
Of 100,165 recalls in the database, 23,668 are high severity, 72,097 moderate, and 4,400 low. This recall is classified moderate severity.
Severity
Moderate
Affected scope
Full Circle: 2,742/12/3/3.3 oz/bags/boxes/cases; Sprouts: 371/12/3/3.3 oz/bags/boxes/cases; Lifesmart: 336/12/3/94 g/bags/boxes/cases
Related Recalls
6
3 from same agency
Buttered microwave popcorn packaged in the following ways: 1) Full Circle Organic Microwave Popcorn Butter, 3-3.3 oz (94 g) bags, Net Wt. 9.9 oz (281 g), Distributed by Topco Associates LLC, Elk Grove Villiage, IL, UPC 36800-40609 2) Sprouts Farmers Market, Organic Butter Microwave Popcorn,3-3.3 oz (94 g) bags, Net Wt. 9.9 oz (281 g), Manufactured Exclusively For Sprouts Farmers Market Phoenix AZ UPC 46670-31919 3) Life Smart Organic Microwave Popping Corn Butter Flavour, 3 bags x 94 g 282 g, Imported For Metro Brands Montreal Quebec, UPC 59749-97319
Popcorn ingredient was recalled due to foreign matter: tempered glass between 3 mm and 7 mm in size
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-1543-2020 |
| Date reported | September 30, 2020 |
| Date initiated | September 9, 2020 |
| Recalling firm | Gilster-Mary Lee Corp. |
| Firm location | Chester, IL |
| Affected scope | Full Circle: 2,742/12/3/3.3 oz/bags/boxes/cases; Sprouts: 371/12/3/3.3 oz/bags/boxes/cases; Lifesmart: 336/12/3/94 g/bags/boxes/cases |
| Distribution | 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 |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
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This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported September 30, 2020.
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records — no number is typed in by an editor. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of June 2026.