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FDAAugust 21, 2015drug

Ipratropium Bromide 0.5 mg and Albuterol Sulfate 3 mg Inhalation Solution, packaged in 30x3 mL Sterile Unit-Dose Vials, a) 30 count (NDC 0487-0201-03) and b) 60 count (NDC 0487-0201-60) vials per carton, Rx only, Nephron Pharmaceutical Corporation, Orlando, FL

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Lack of Assurance of Sterility; potential exposure to non-sterile lubricant during the filling process

What to do

FDA enforcement status: Terminated

Brands named

nephron pharmaceuticalsnephron

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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