DrugAug 5, 2020
MasterPharm Formula 82M recall — FDA D-1424-2020
Lack of Processing Controls (lack of assurance of conformity to specifications).
Class IIFDA: TerminatedMasterPharm LLC
Recall history in this database
Classification mix: Class I: 2, Class II: 1.
DrugJul 8, 2020
MasterPharm Minoxidil/Biotin/Spironolactone 1.25/5/25 mg capsule, 90 capsules per bottle recall — FDA D-1363-2020
Super-potent Drug: This recall has been initiated due to the elevated presence of minoxidil and biotin.
Class IFDA: TerminatedMasterPharm LLC
DrugMay 20, 2020
MasterPharm Finasteride Plus 1.25 mg Capsule, a) 30-count bottle, b) 90-count bottle recall — FDA D-1269-2020
Cross Contamination with Other Products; Finasteride Plus 1.25mg capsules were found to contain minoxidil.
Class IFDA: TerminatedMasterPharm LLC
Understanding this recall history
This page summarizes recall records in which the official source identifies MasterPharm LLC 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.