AstraZeneca LP recalls PULMICORT RESPULES 0.25 mg/2 ml Budesonide Inhalation Suspension (30 ampules/carton) NDC: 0186-1988-04
Recalled March 20, 2013 · FDA recall D-198-2013 · AstraZeneca
Hazard
Does Not Meet Monograph: Budesonide may be slightly above or below the specification range. · FDA Class III
Units
28,476 cartons
Sold at
Nationwide
Description
Does Not Meet Monograph: Budesonide may be slightly above or below the specification range.
Product
PULMICORT RESPULES 0.25 mg/2 ml Budesonide Inhalation Suspension (30 ampules/carton) NDC: 0186-1988-04
Manufacturer(s)
AstraZeneca LP
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →