PlainRecalls
FDA Drug Moderate Class II Terminated

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.

Reported: August 15, 2012 Initiated: June 22, 2011 #D-1446-2012

Product Description

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.

Reason for Recall

Lack of Assurance of Sterility

Details

Units Affected
56,028 cartons
Distribution
Nationwide and Puerto Rico
Location
Orlando, FL

Frequently Asked Questions

What product was recalled?
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.. Recalled by Nephron Pharmaceuticals Corp.. Units affected: 56,028 cartons.
Why was this product recalled?
Lack of Assurance of Sterility
Which agency issued this recall?
This recall was issued by the FDA Drug on August 15, 2012. Severity: Moderate. Recall number: D-1446-2012.