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Policy version 2026-07-21, effective July 21, 2026.
United States
TerminatedClass II
Popcorn ingredient was recalled due to foreign matter: tempered glass between 3 mm and 7 mm in size
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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 | 36800-40611 | 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 | Full Circle: AUG1821N2, JUL1621N2, JUL1721N2, JUL2021N2, JUL3121N2; Sprouts: JUL1721N2; Lifesmart: BB/MA 20210716N2 Nature's Promise:AUG0121N2, AUG1821N2, JUL1821N2, JUL2021N2, JUL2321N2, JUL2721N2, JUL3121N2; |
This recall shares FDA event ID 86397 with 4 other product entries in Public Health Trace.
FDA Recall United States TerminatedTerminated: December 8, 2020Historical recordClass II
FDA Recall United States TerminatedTerminated: December 8, 2020Historical recordClass II
FDA Recall United States TerminatedTerminated: December 8, 2020Historical recordClass II
FDA Recall United States TerminatedTerminated: December 8, 2020Historical recordClass II
Responsible company: Gilster-Mary Lee Corp.
FDA Recall United States TerminatedTerminated: May 17, 2023Historical recordClass I
FDA Recall United States TerminatedTerminated: July 19, 2021Historical recordClass I
FDA Recall United States TerminatedTerminated: December 8, 2020Historical recordClass II
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Arizona | 1 |
| California | 1 |
| Connecticut | 1 |
| Florida | 1 |
| Louisiana | 1 |
| Massachusetts | 1 |
| Maryland | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| North Carolina | 1 |
| New Hampshire | 1 |
| New York | 1 |
| Ohio | 1 |
| Pennsylvania | 1 |
| Texas | 1 |
| Utah | 1 |
| Virginia | 1 |
| Vermont | 1 |
| Washington | 1 |
| Wisconsin | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
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