FDA Recall United States TerminatedTerminated: February 12, 2019Historical recordClass I
Fieldbrook Foods Corporation
- Product
- RASPBERRY Cream Ice Cream Bars: Sundae SHOPPE, 12 Bars, UPC…
- Published
- January 24, 2018
- Distribution
- Nationwide
United States
TerminatedClass I
Product may be contaminated with Listeria monocytogenes.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Ice Cream Variety Packs containing Sandwiches, Bars, and Cones, Sold under the following: 30 pack - pics BY PRICE CHOPPER - UPC: 041735080295; STARTER BROS Ice Cream Favorites Variety Pack, UPC: 074175850111; WELLSLEY FARMS ICE CREAM TREATS VARIETY PACK, UPC: 888670020487; STONE RIDGE CREAMERY CLASSIC VARIETY PACK, UPC: 041130614330; POLAR EXPRESS ICE CREAM COMPANY Variety Pack, UPC: 071632613692; GIANT EAGLE Variety Pack, UPC: 030034065676; Food Club VARIETY PACK, UPC: 036800415249; FIRST STREET Ice Cream Variety Pack, UPC: 041512138690 and 32 pack - weis quality ice cream variety pack, UPC: 041497010554 | 041735080295 | 639,900 cases (total for all products) | The recalled products have a production date of January 1, 2017 to December 31, 2017 and a best by date of January 1, 2018 to December 31, 2018. The Hood and Kemps products may show a best by date of July 1, 2018 to June 30, 2019. |
This recall shares FDA event ID 78876 with 3 other product entries in Public Health Trace.
FDA Recall United States TerminatedTerminated: February 12, 2019Historical recordClass I
FDA Recall United States TerminatedTerminated: February 12, 2019Historical recordClass I
FDA Recall United States TerminatedTerminated: February 12, 2019Historical recordClass I
Responsible company: Fieldbrook Foods Corporation
FDA Recall United States TerminatedTerminated: February 12, 2019Historical recordClass I
FDA Recall United States TerminatedTerminated: February 12, 2019Historical recordClass I
FDA Recall United States TerminatedTerminated: February 12, 2019Historical recordClass I
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 |
|---|---|
| Massachusetts | 1 |
| Illinois | 1 |
| California | 1 |
| Puerto Rico | 1 |
| Florida | 1 |
| Minnesota | 1 |
| Ohio | 1 |
| Connecticut | 1 |
| Michigan | 1 |
| Missouri | 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 I. 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 February 12, 2019.
Status as reported: Terminated.
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