CutisPharma, Inc. Recalls

Overview of recall records associated with CutisPharma, Inc., including dates, categories and classifications where available.

2recall records

Nov 23, 2016latest record date

Nov 23, 2016earliest record date

Recall history in this database

Classification mix: Class III: 2.

DrugNov 23, 2016

CutisPharma FIRST Omeprazole 2mg/mL in FIRST PPI Suspension Compounding Kit , 3 OZ recall — FDA D-0139-2017

Labeling: Label error on declared strength. Package Insert -Error in the Description section of the package insert refers to the strength as 3mg per mL; however it should state 2mg per mL

Class IIIFDA: TerminatedCutisPharma, Inc.

DrugNov 23, 2016

CutisPharma FIRST Omeprazole 2mg/mL in FIRST PPI Suspension Compounding Kit , 5 oz recall — FDA D-0138-2017

Labeling: Label error on declared strength. Package Insert -Error in the Description section of the package insert refers to the strength as 3mg per mL; however it should state 2mg per mL

Class IIIFDA: TerminatedCutisPharma, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies CutisPharma, 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.