FDAFDA · Food and drugs·Recall number D-198-2013
PULMICORT RESPULES 0.25 mg/2 ml Budesonide Inhalation Suspension (30 ampules/carton) NDC: 0186-1988-04
Published March 20, 2013 · Recall initiated: January 11, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Does Not Meet Monograph: Budesonide may be slightly above or below the specification range.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- PULMICORT RESPULES
- Manufacturer
- AstraZeneca LP
- Distributor
- Nationwide
- Lot
- Lot/Exp date: AH0054 Exp 5/14; AK0125 Exp 7/14
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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