AstraZeneca LP
AstraZeneca LP appears in FDA public data with 2 recalls, 0 510(k) clearances, 32 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-198-2013, Class III) was initiated on January 11, 2013.
Summary
- Total Recalls
- 2
- 510(k) Clearances
- 0
- Inspections
- 32
- Compliance Actions
- 0
Known Names
astrazeneca, astrazeneca pharmaceuticals, astrazeneca r and d molndal, astrazeneca r and d
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| D-198-2013 | Class III | PULMICORT RESPULES 0.25 mg/2 ml Budesonide Inhalation Suspension (30 ampules/carton) NDC: 0186-1 | January 11, 2013 |
| D-199-2013 | Class III | PULMICORT RESPULES 0.5 mg/2 ml (30 ampules/carton) Budesonide Inhalation Suspension NDC: 0186-1989 | January 11, 2013 |