Recall record at a glance
| Official record | F-0001-2019 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Lamb Weston Inc. |
| Report date | Oct 10, 2018 |
| Recall initiation date | Sep 20, 2018 |
| Quantity | Brookshire = 2075 cases; Market Pantry = 3954 cases; Hill Country Fare Breakfast = 864 cases; Stater Bros = 1166 cases |
| Location | Richland, WA, United States |
Official product description
Formed Hash Brown Patties, packaged in cardboard trays covered with plastic film, frozen products. The following brands are subject to this recall. ***Brookshire's Golden Hash Brown Patties. Firm and address listed on label: "Brookshire Grocery Company PO Box 1411 Tyler, TX 75710-1411". -Tray UPC 0 92825 09630 6, retail packaged in 22.5 OZ (1 LB 6.5 OZ) 638g. -Case Item 09630, case UPC 1 00 92825 09630 3, case net wt. 16.8 LB (7.6 kg). ***Market Pantry Hash Brown Patties. Firm and address listed on label: "Dist. By Target Corporation Minneapolis, MN 55403". -Tray UPC 0 85239 01079 2, retail packaged in 22.5 OZ (1 LB 6.5 OZ) 637g. -Case item MP079, case UPC 2 00 85239 01079 6, case net wt. 16.87 LB (7.65 kg). ***Hill Country Fare Breakfast Hash Browns Potato Patties. Firm and address listed on label: "H-E-B San Antonio, Texas 78204". -Tray UPC 0 41220 90938 4, retail packaged in 45 OZ (2 LB 13 OZ) / CONT.NET. 1.27kg. -Case item H9400, case UPC 1 00 41220 90938 1, case net wt. 33.7 LB (15.2 kg). ***Stater Bros. Hash Brown Patties Shredded Potatoes. Firm and address listed on label: "Stater Bros. Markets San Bernardino, CA 92408" -Tray UPC 0 74175 50486 1, retail packaged in 45 OZ (2LB 13OZ) 1.27KG. -Case item # 50486, case UPC 1 00 74175 50486 8, case net wt. 33.75 LB (15.3 kg).
Why the product was recalled
Hash brown product, sold under brands Brookshire's, Market Pantry, Breakfast, and Stater Bros, are recalled because the product may contain small fragments of hard, clear plastic.
Distribution information
CA, FL, IA, MA, MD, OH, PA, and TX.
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA 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.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.