🔍 RecallPedia

PULMICORT RESPULES 0.25 mg/2 ml Budesonide Inhalation Suspension (30 ampules/carton) NDC: 0186-1988-04

Class I - Dangerous
💊 Drugs Recalled: January 11, 2013 AstraZeneca Other Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot/Exp date: AH0054 Exp 5/14; AK0125 Exp 7/14
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
AstraZeneca LP
Reason for Recall:
Does Not Meet Monograph: Budesonide may be slightly above or below the specification range.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

PULMICORT RESPULES 0.25 mg/2 ml Budesonide Inhalation Suspension (30 ampules/carton) NDC: 0186-1988-04

Product Codes/Lot Numbers:

Lot/Exp date: AH0054 Exp 5/14; AK0125 Exp 7/14

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-198-2013

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