Ipratropium Bromide recalls
The FDA has published 6 recalls involving Ipratropium Bromide since 2015. The latest was reported on 1 May 2024. Most were for sterility. Mckesson Medical-Surgical Inc. Corporate Office has the most recalls in this group. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls6since 2015
Last 12 months0reported
Class I00% of total
Ongoing0latest 1 May 2024
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 5 83%Class III 1 17%
Why ipratropium bromide is recalled
Companies
Brands
By year
All ipratropium bromide recalls, newest first
6 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Ipratropium Bromide and Albuterol Sulfate Inhalation recalledIpratropium Bromide And Albuterol Sulfate | Cipla USA | Packaging Defects | Nationwide |
| Drug | CLASS II | Ipratropium Bromide and Albuterol Sulfate Inhalation recalledIpratropium Bromide And Albuterol Sulfate | Cardinal Healthcare | Sterility | Nationwide |
| Drug | CLASS III | Ipratropium Bromide 5 mg and Albuterol Sulfate 3 mg recalledIpratropium Bromide And Albuterol Sulfate | Mckesson Medical-Surgical Inc. Corporate Office | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Ipratropium Bromide Inhalation Solution, 02%, 5 mg recalledIpratropium Bromide | Mckesson Medical-Surgical Inc. Corporate Office | Sterility | Nationwide |
| Drug | CLASS II | Ipratropium Bromide 5 mg and Albuterol Sulfate 3 mg recalledIpratropium Bromide And Albuterol Sulfate | Nephron Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Combivent Respimat (ipratropium bromide recalledCombivent Respimat | Boehringer Ingelheim Roxane | Other | Nationwide |
Should you stop taking Ipratropium Bromide?
Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.