FDA recall record

Fieldbrook Foods Orange Cream Ice Cream Bars sold under the following labels recall — FDA F-0684-2018

Product may be contaminated with Listeria monocytogenes.

Class Iclassification
F-0684-2018official record ID
Jan 24, 2018report date

Recall record at a glance

Official recordF-0684-2018
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmFieldbrook Foods Corporation
Report dateJan 24, 2018
Recall initiation dateJan 3, 2018
Quantity639,900 cases (total for all products)
LocationDunkirk, NY, United States

Official product description

Orange Cream Ice Cream Bars sold under the following labels: Sold in a 12-pack: Ahold UPC: 6 88267 03292 9, Econo UPC: 7 08938 00610 0, First Street no OCB s, Food Club UPC: 7 08938 00610 0, Giant Eagle UPC: 0 30034 00337 1, Great Value no OCB s, Greens UPC: 0 71441 03130 4, Hagan UPC: 0 37498 01609 1, Hood UPC: 0 44100 23138 4, Kemps UPC: 0 41483 03806 7, Kroger UPC: 0 11110 57028 4, Lucerne UPC: 0 21130 09796 8, Market Basket UPC: 0 49705 96901 4, PIC - no product of ours, Polar Express Only Variety pack, Price Rite UOPC: 0 41190 75722 0, Price Chopper UPC: 0 41735 09372 1, Purple Cow UPC: 7 08820 42753 2, Shoprite UPC: 0 41190 40125 3, Southern Home UPC: 6 07880 01142 5, Stater UPC: 0 74175 85013 5, Stoneridge UPC: 0 41130 61419 4, Sundae Shoppe UPC: 0 41498 8642 5, Tops UPC: 0 70784 04916 8, United Dairy UPS: 0 71580 08092 8, Weis UPC: 0 41497 01108 7, Wellsley Farms Only Variety pack, Winn Dixie no OCB s, Worlds Fair UPC: 0 51933 06140 8 and sold in a 3 pack - Party Treat UPC: 0 71632 00235 9

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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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