FDA Recall D-1269-2020
MasterPharm LLC · South Richmond Hill, NY
Class I — life-threatening Terminated 1241 days on record
Highest impact — Class I recall — FDA determination of strong likelihood of serious adverse health consequence or death.
Product
Finasteride Plus 1.25 mg Capsule, a) 30-count bottle, b) 90-count bottle, Compounded Product Not for Resale, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419.
Reason for recall
Cross Contamination with Other Products; Finasteride Plus 1.25mg capsules were found to contain minoxidil.
Recall record
- Recall number
D-1269-2020- Classification
- Class I
- Status
- Terminated
- Voluntary or mandated
- Voluntary: Firm initiated
- Firm notification
- Telephone
- Distribution
- Nationwide in the U.S.
- Recall initiated
- 2020-04-14
- Classified by FDA Center
- 2020-05-19
- FDA published
- 2020-05-20
- Terminated
- 2023-09-07
- Recalling firm
- MasterPharm LLC
- Firm location
- South Richmond Hill, NY