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Nephron Pharmaceuticals Recalls
10 recalls on record · August 15, 2012 to July 6, 2016 · Drugs, Medical Devices
Recalls by year
12
13
15
16
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
Also filed under
The recall feeds record what looks like the same company under more than one name:
July 6, 2016Medical DevicesFDA
Nephron Pharmaceuticals Corp. recalls Sodium Chloride Inhalation Solution, USP 7%, 60 x 4 mL Sterile Unit-Dose Vials, Rx Only, NDC 0487-9007-60. A vial conta
Hazard: Lack of Assurance of Sterility: Internal dye ingress test failure to assure the integrity of the vial.
July 6, 2016Medical DevicesFDA
Nephron Pharmaceuticals Corp. recalls Sodium Chloride Inhalation Solution, USP 3%, 60 x 4 mL Sterile Unit-Dose Vials per carton, Rx Only, NDC 0487-9003-60.
Hazard: Lack of Assurance of Sterility: Internal dye ingress test failure to assure the integrity of the vial.
December 9, 2015DrugsFDA
Nephron Pharmaceuticals Corp. recalls Asthmanefrin Racepinephrine Inhalation Solution Bronchodilator Refills (Racepinephrine USP 11.25 mg), 30 individual foi
Hazard: Discoloration
December 9, 2015DrugsFDA
Nephron Pharmaceuticals Corp. recalls Asthmanefrin Racepinephrine Inhalation Solution Bronchodilator, Starter Kit (Racepinephrine 11.25 mg) 10 individual foil
Hazard: Discoloration
October 21, 2015DrugsFDA
Nephron Pharmaceuticals Corp. recalls Ipratropium Bromide 0.5 mg and Albuterol Sulfate 3 mg Inhalation Solution, packaged in 30x3 mL Sterile Unit-Dose Vials,
Hazard: Lack of Assurance of Sterility; potential exposure to non-sterile lubricant during the filling process
October 30, 2013DrugsFDA
Nephron Pharmaceuticals Corp. recalls Albuterol Sulfate Inhalation Solution, 0.083% 2.5 mg/3 mL for Oral Inhalation Only, Rx Only, 25 x 3 mL Sterile Unit-Dos
Hazard: Lack of Assurance of Sterility: Nephron Pharmaceuticals Corporation conducted a routine periodic aseptic process simulation and discovered bacterial growth in a number of media fill vials, exceeding the allowable limit.
June 5, 2013Medical DevicesFDA
Nephron Pharmaceuticals Corp. recalls EZ Breathe Medication Cup. For the delivery of liquid medications for respiratory usage.
Hazard: Possible dislodgement of the "Plate A", if this instance occurs, it presents a potential choking hazard.
June 5, 2013Medical DevicesFDA
Nephron Pharmaceuticals Corp. recalls AsthmaNefrin Starter Kit contains ten (10) AsthmaNefrin vials and one (1) EZ Breathe Atomizer. For the delivery of li
Hazard: Possible dislodgement of the "Plate A", if this instance occurs, it presents a potential choking hazard.
June 5, 2013Medical DevicesFDA
Nephron Pharmaceuticals Corp. recalls EZ Breathe Atomizer Model # EZ-100. For the delivery of liquid medications for respiratory usage.
Hazard: Possible dislodgement of the "Plate A", if this instance occurs, it presents a potential choking hazard.
August 15, 2012DrugsFDA
Nephron Pharmaceuticals Corp. recalls Albuterol Sulfate Inhalation Solution, 0.083%, 2.5 mg/3 mL Sterile Unit-Dose Vials, 60-count (60 x 3 mL Sterile Unit-Dos
Hazard: Lack of Assurance of Sterility