AstraZeneca LP recalls PULMICORT RESPULES 0.5 mg/2 ml (30 ampules/carton) Budesonide Inhalation Suspension NDC: 0186-1989-04
Recalled March 20, 2013 · FDA recall D-199-2013 · AstraZeneca
Hazard
Does Not Meet Monograph: Budesonide may be slightly above or below the specification range. · FDA Class III
Units
64675 cartons
Sold at
Nationwide
Description
Does Not Meet Monograph: Budesonide may be slightly above or below the specification range.
Product
PULMICORT RESPULES 0.5 mg/2 ml (30 ampules/carton) Budesonide Inhalation Suspension NDC: 0186-1989-04
Manufacturer(s)
AstraZeneca LP
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →