Recall record at a glance
| Official record | F-0132-2020 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Pride of Iowa Sandwiches, Inc. |
| Report date | Nov 13, 2019 |
| Recall initiation date | Oct 29, 2019 |
| Quantity | 633 cases/7596 units |
| Location | Marengo, IA, United States |
Official product description
Market Choice Monster Cheeseburger, Net Wt. 9.1 oz individually wrapped in plastic, packaged 12 count per case.
Why the product was recalled
The firm received a recall notice for an ingredient, ready-to-eat beef patties, which were potentially contaminated with foreign metal material. The patties were used in the manufacture of sandwiches.
Distribution information
Distributed to food vending distributors in Michigan and Texas
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: E-Mail.
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.