Wienke LLC
Recall History
| Date | Product | Class | Status |
|---|---|---|---|
| Jan 19, 2018 | Wienke's Market Strawberry Raspberry Jam, Net Wt. 8 oz (2... | Class II | Terminated |
| Jan 19, 2018 | Wienke's Market Cherry Rhubarb Jam, Net Wt. 8 oz (226g), ... | Class II | Terminated |
| Jan 19, 2018 | Wienke's Market Strawberry Cherry Jam, Net Wt. 8 oz (226g... | Class II | Terminated |
| Jan 19, 2018 | Wienke's Market Strawberry Banana Jam, Net Wt. 8 oz (226g... | Class II | Terminated |
| Jan 19, 2018 | Wienke's Market Cherry Blueberry Jam, Net Wt. 8 oz (226g)... | Class II | Terminated |
| Jan 19, 2018 | Wienke's Market No Sugar Added Raspberry Jam, Net Wt. 8 ... | Class II | Terminated |
| Jan 19, 2018 | Wienke's Market No Sugar Added Cherry Rhubarb Jam, Net W... | Class II | Terminated |
| Jan 19, 2018 | Wienke's Market Apricot Jam, Net Wt. 8 oz (226g), UPC 141... | Class II | Terminated |
| Jan 19, 2018 | Wienke's Market No Sugar Added Summer Blend Jam, Net Wt.... | Class II | Terminated |
| Jan 19, 2018 | Wienke's Market Blueberry Jam, Net Wt. 8 oz (226g), UPC 1... | Class II | Terminated |
Recall data sourced from the FDA's recalls and safety alerts database. Class I recalls indicate a reasonable probability of serious adverse health consequences. Always check the USDA FSIS recall list for meat and poultry products.
Frequently Asked Questions
Yes, Wienke LLC has 10 FDA food recalls on record, including 0 Class I (dangerous) recalls. There are no active recalls at this time.
Wienke LLC has no active recalls at this time. However, the brand has 10 historical recalls. Always check this page for the latest recall status.
Wienke LLC's 10 recalls break down by severity: 0 Class I (may cause serious health issues), 10 Class II (may cause temporary health problems), and 0 Class III (unlikely to cause harm). See the full recall history table above for specific reasons.
Wienke LLC recalls have affected AL, AK, IL, IA, MI, MN, OR, PA, UT, WI. Check individual recall entries for specific distribution details.
Related
Recall data is sourced from the FDA openFDA enforcement database. Classifications reflect FDA severity ratings: Class I (dangerous), Class II (may cause temporary health problems), Class III (unlikely harmful).