Maximum Strength Cough And Chest Congestion And Nighttime Severe Cold And Flu Combo Pack recalls
Maximum Strength Cough And Chest Congestion And Nighttime Severe Cold And Flu Combo Pack products have been recalled 2 times, most recently on 13 Nov 2024. The recalling company is usually Denison Pharmaceuticals. The most common reason is packaging defects.
Total recalls2since 2024
Last 12 months0reported
Class I00% of total
Ongoing2latest 13 Nov 2024
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 0 0%Class III 2 100%
Why maximum strength cough and chest congestion and nighttime severe cold and flu combo pack is recalled
Companies
Product types
By year
Ongoing maximum strength cough and chest congestion and nighttime severe cold and flu combo pack recalls
2 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Kids' Cough and Chest Congestion (Dextromethorphan HBr recalledMaximum Strength Cough And Chest Congestion And Nighttime Severe Cold And Flu Combo Pack | Denison Pharmaceuticals | Packaging Defects | RI |
| Drug | CLASS III | Adult Cough and Chest Congestion recalled by Denison PharmaceuticalsMaximum Strength Cough And Chest Congestion And Nighttime Severe Cold And Flu Combo Pack | Denison Pharmaceuticals | Packaging Defects | RI |
All maximum strength cough and chest congestion and nighttime severe cold and flu combo pack recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Kids' Cough and Chest Congestion (Dextromethorphan HBr recalledMaximum Strength Cough And Chest Congestion And Nighttime Severe Cold And Flu Combo Pack | Denison Pharmaceuticals | Packaging Defects | RI |
| Drug | CLASS III | Adult Cough and Chest Congestion recalled by Denison PharmaceuticalsMaximum Strength Cough And Chest Congestion And Nighttime Severe Cold And Flu Combo Pack | Denison Pharmaceuticals | Packaging Defects | RI |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.