SCA Pharmaceuticals Furosemide 100 mg added to 0.9% Sodium Chloride 100 mL Injection, 100 mL recall — FDA D-1189-2018
Presence of Precipitate: Customer complaint for visible precipitate in product believed to be the active ingredient furosemide.
Overview of recall records associated with SCA Pharmaceuticals, Inc., including dates, categories and classifications where available.
Classification mix: Class I: 1.
Presence of Precipitate: Customer complaint for visible precipitate in product believed to be the active ingredient furosemide.
This page summarizes recall records in which the official source identifies SCA Pharmaceuticals, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.