PULMICORT RESPULES 0.25 mg/2 ml Budesonide Inhalation recall
PULMICORT RESPULES 0.25 mg/2 ml Budesonide Inhalation Suspension (30 ampules/carton) NDC: 0186-1988-04
Why was PULMICORT RESPULES 0.25 mg/2 ml Budesonide Inhalation recalled?
Does Not Meet Monograph: Budesonide may be slightly above or below the specification range.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot/Exp date: AH0054 Exp 5/14; AK0125 Exp 7/14
- Product
- PULMICORT RESPULES 0.25 mg/2 ml Budesonide Inhalation Suspension (30 ampules/carton) NDC: 0186-1988-04
- Recalling firm
- AstraZeneca LP
- Quantity
- 28,476 cartons
- Distribution
- Nationwide
- Recall date
- March 20, 2013
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)