FDAFDA · Food and drugs·Recall number D-1446-2012
Albuterol Sulfate Inhalation Solution, 0.083%, 2.5 mg/3 mL Sterile Unit-Dose Vials, 60-count (60 x 3 mL Sterile Unit-Dose Vials) per carton, Rx only, Manufactured by: nephron pharmaceuticals corporation, Orlando, FL 32811, NDC 0487-9501-60.
Published August 15, 2012 · Recall initiated: June 22, 2011
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
Lack of Assurance of Sterility
What to do
Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recall details
- Brand
- ALBUTEROL SULFATE
- Manufacturer
- Nephron Pharmaceuticals Corp.
- Distributor
- Nationwide and Puerto Rico
- UPC
- 0304879501003
- Lot
- Lot #: A0654A, Exp 07/12; A0A62A, Exp 10/12
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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