Sentara Enterprises PENICILLIN in D5W, Packaged as a)36MU in 360ML Homepumps and b) 51MU in recall — FDA D-0632-2016
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Complete FDA and NHTSA recall records dated in February 2016.
These records include useful source details for the selected month.
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Labeling: Incorrect or Missing Package Insert: Package insert is missing updates compared with reference drug insert.
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Defective Delivery System: Firm recalled Guaifenesin liquid and Guaifenesin DM liquid due incorrect dose markings on the dosing cups.
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.