DrugDec 27, 2017
Claris Lifesciences Ciprofloxacin in Dextrose (5%) Injection, USP 200 mg in 100 mL 5% recall — FDA D-0127-2018
Superpotent
Class IIIFDA: TerminatedClaris Lifesciences Inc.
Recall history in this database
Classification mix: Class II: 4, Class III: 1.
DrugApr 5, 2017
Claris Lifesciences Fluconazole Injection, USP, 400 mg in 200 mL recall — FDA D-0614-2017
Lack of Assurance of Sterility: there is potential of a leak from the primary container which may result in a potential breach of sterility and contamination of the product.
Class IIFDA: TerminatedClaris Lifesciences Inc.
DrugApr 5, 2017
Levofloxacin Injection in 5% Dextrose, 750 mg in 150 mL 5% Dextrose recall — FDA D-0615-2017
Lack of Assurance of Sterility: there is potential of a leak from the primary container which may result in a potential breach of sterility and contamination of the product.
Class IIFDA: TerminatedClaris Lifesciences Inc.
DrugApr 5, 2017
Claris Lifesciences Ciprofloxacin in Dextrose (5%) Injection, USP, 400 mg in 200 mL 5% recall — FDA D-0613-2017
Lack of Assurance of Sterility: there is potential of a leak from the primary container which may result in a potential breach of sterility and contamination of the product.
Class IIFDA: TerminatedClaris Lifesciences Inc.
DrugApr 5, 2017
Claris Lifesciences Metronidazole Injection, USP, 500 mg/100 mL recall — FDA D-0616-2017
Lack of Assurance of Sterility: there is potential of a leak from the primary container which may result in a potential breach of sterility and contamination of the product.
Class IIFDA: TerminatedClaris Lifesciences Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies Claris Lifesciences 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.