Pulmicort Respules recalls
Pulmicort Respules products have been recalled 2 times, most recently on 20 Mar 2013. The recalling company is usually AstraZeneca.
Total recalls2since 2013
Last 12 months0reported
Class I00% of total
Ongoing0latest 20 Mar 2013
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 pulmicort respules is recalled
Companies
Product types
By year
All pulmicort respules recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Pulmicort Respules 25 mg/ Budesonide Inhalation Suspension recalledPulmicort Respules | AstraZeneca | Other | Nationwide |
| Drug | CLASS III | Pulmicort Respules 5 mg/ (30 ampules/carton) Budesonide recalledPulmicort Respules | AstraZeneca | Other | Nationwide |
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.