Cantrell Drug Company Oxytocin 30 USP Units Added to 0.9% Sodium Chloride, 500 mL Bag recall — FDA D-0201-2017
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Overview of recall records associated with Cantrell Drug Company, including dates, categories and classifications where available.
Classification mix: Class II: 19.
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
This page summarizes recall records in which the official source identifies Cantrell Drug Company 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.