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Nephron Pharmaceuticals Corp.: Medical Device Recalls in 2016

Updated on March 25, 2026.

According to to data from the FDA, there were 2 medical device recalls made by Nephron Pharmaceuticals Corp. in 2016. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.
See this for other years:
2013
2016
  • Sodium Chloride Inhalation Solution, USP 7%, 60 x 4 mL Sterile Unit-Dose Vials, Rx Only, NDC 0487-9007-60. A vial contains sterile, preservation-free, clear, colorless, aqueous solution as labeled for induction of sputum production where specimen collection is indicated. For respiratory therapy, Solium Chloride Inhalation Solution USP, 3% is used in conjunction with a nebulizer
  • Sodium Chloride Inhalation Solution, USP 3%, 60 x 4 mL Sterile Unit-Dose Vials per carton, Rx Only, NDC 0487-9003-60. A vial contains sterile, preservation-free, clear, colorless, aqueous solution as labeled for induction of sputum production where specimen collection is indicated. For respiratory therapy, Solium Chloride Inhalation Solution USP, 3% is used in conjunction with a nebulizer
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