Recall record at a glance
| Official record | F-1851-2018 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Pacific Coast Fruit Company |
| Report date | Aug 29, 2018 |
| Recall initiation date | Aug 16, 2018 |
| Quantity | 126 Cases |
| Location | Portland, OR, United States |
Official product description
Spinach Chopped 1", item # 73039. packaged in plastic bag, each case contains 2/5# bags, There are case labels and no unit label. UPC on case label 0 20728 73039. The case label is read in part: "***SPINACH CHOPPED 1" *** 2/5#***73039***PACIFIC COAST FRUIT, PORTLAND, OR 97232***Keep Refrigerated***.
Why the product was recalled
Product is recalled due to a potential contamination with Cyclospora.
Distribution information
Distributed in OR
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: Telephone.
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.