Recalls / Brands / Ipratropium Bromide And Albuterol Sulfate
Ipratropium Bromide And Albuterol Sulfate
4 FDA drug recalls involving brand “Ipratropium Bromide And Albuterol Sulfate”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2024-03-26 | Class II | Ipratropium Bromide and Albuterol Sulfate Inhalation Solution USP, 0.5 mg & 3mg/3mL unit-dose vials, packaged | Cipla USA, Inc. |
| 2022-04-13 | Class III | Ipratropium Bromide 0.5 mg and Albuterol Sulfate 3 mg Inhalation Solution 3mL vial, packaged in a) 30-count | Mckesson Medical-Surgical Inc. Corporate Office |
| 2022-01-26 | Class II | Ipratropium Bromide and Albuterol Sulfate Inhalation Solution (0.5 mg/3 mg per 3 mL), 60 x 3 mL Sterile Unit-D | CARDINAL HEALTHCARE |
| 2015-08-21 | Class II | Ipratropium Bromide 0.5 mg and Albuterol Sulfate 3 mg Inhalation Solution, packaged in 30x3 mL Sterile Unit-Do | Nephron Pharmaceuticals Corp. |