FDA Recall United States TerminatedTerminated: November 28, 2018Historical recordClass II
Kemps, LLC
- Product
- Kemps Sweet Me Creamery Maple Toffee Blondie, One Pint, UPC…
- Published
- May 24, 2017
- Distribution
- AL, CA, FL, IA, IL, LA, MA, MD, MI, MN,…
United States
TerminatedClass II
Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2 Frozen Yogurt because they may contain pieces of plastic.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Kemps Sweet Me Creamery Creamy Dark Chocolate Mint, One Pint, UPC 41483-04143 | 41483-04143 | 91,672 units Ice Cream | Sell By Dates: 7/6/2018, 7/7/2018, 7/25/2018 |
This recall shares FDA event ID 77091 with 9 other product entries in Public Health Trace.
FDA Recall United States TerminatedTerminated: November 28, 2018Historical recordClass II
FDA Recall United States TerminatedTerminated: November 28, 2018Historical recordClass II
FDA Recall United States TerminatedTerminated: November 28, 2018Historical recordClass II
FDA Recall United States TerminatedTerminated: November 28, 2018Historical recordClass II
FDA Recall United States TerminatedTerminated: November 28, 2018Historical recordClass II
FDA Recall United States TerminatedTerminated: November 28, 2018Historical recordClass II
FDA Recall United States TerminatedTerminated: November 28, 2018Historical recordClass II
FDA Recall United States TerminatedTerminated: November 28, 2018Historical recordClass II
FDA Recall United States TerminatedTerminated: November 28, 2018Historical recordClass II
Responsible company: Kemps, LLC
FDA Recall United States TerminatedTerminated: February 8, 2019Historical recordClass I
FDA Recall United States TerminatedTerminated: November 28, 2018Historical recordClass II
FDA Recall United States TerminatedTerminated: November 28, 2018Historical 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 |
|---|---|
| Alabama | 1 |
| California | 1 |
| Florida | 1 |
| Iowa | 1 |
| Illinois | 1 |
| Louisiana | 1 |
| Massachusetts | 1 |
| Maryland | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| North Carolina | 1 |
| North Dakota | 1 |
| New Jersey | 1 |
| New York | 1 |
| Pennsylvania | 1 |
| South Carolina | 1 |
| Texas | 1 |
| Virginia | 1 |
| Vermont | 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.
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View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
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This record is preserved as published by FDA, as of November 28, 2018.
Status as reported: Terminated.
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