Recall record at a glance
| Official record | F-0685-2018 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Fieldbrook Foods Corporation |
| Report date | Jan 24, 2018 |
| Recall initiation date | Jan 3, 2018 |
| Quantity | 639,900 cases (total for all products) |
| Location | Dunkirk, NY, United States |
Official product description
Chocolate Covered Vanilla Ice Cream Bars packaged under the following brands: 12 packs - Ahold UPC: 6 88267 03323 5 and different ICB: 6 88267 08587 1, Econo UPC: 7 08938 00534 9, First Street UPC: 0 41512 11933 0, Food Club UPC: 0 36800 78404 8, Giant Eagle UPC: 0 30034 00329 6, Great Value UPC: 0 78742 09158 7, Greens UPC: 0 71441 03131 1, Hagan no ICBs, Hood UPC: 0 44100 23704 1, Kroger UPC: 0 11110 57120 5 and Kroger NFA ICBs UPC: 0 11110 57885 3, Lucerne UPC: 0 21130 09799 9, Market Basket UPC: 0 49705 96902 1, Party Treat No ICBs, PIC no product of ours, Polar Express Only Variety pack, Price Chopper UPC: 0 41735 09260 1, Price Rite UPC: 0 41190 75712 1, Purple Cow UPC: 7 08820 42754 9, Shoprite UPC: 0 41190 40126 0, Southern Home UPC: 6 07880 01147 0, , Stater UPC: 0 74175 85045 6, Stoneridge UPC: 0 41130 61333 3, Sundae Shoppe UPC: 0 41498 17991 5, Tops UPC: 0 70784 04912 0, United Dairy UPC: 0 71580 08079 9, Weis UPC: 0 41497 01042 4, Wellsley Farms Only Variety pack, Winn Dixie UPC: 0 21140 27145 7, World s Fair UPC: 0 51933 67170 6
Why the product was recalled
Product may be contaminated with Listeria monocytogenes.
Distribution information
Sold to distributors in: MA, IL, CA, PR, CA, FL, MN, IL, OH, CT, MI, MO. Product was distributed nationwide including Puerto Rico.
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement 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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