D-1424-2020 Class II Terminated
FDA drug recall D-1424-2020 was initiated by MasterPharm LLC on Jul 2, 2020 and is designated Class II. Reason for recall: Lack of Processing Controls (lack of assurance of conformity to specifications). The recall status is terminated (terminated Feb 23, 2024). Affected quantity: 543 units.
Recall Details
- Product Type
- Drugs
- Report Date
- Aug 5, 2020
- Initiation Date
- Jul 2, 2020
- Termination Date
- Feb 23, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 543 units
Product Description
Formula 82M (Minoxidil 5%/Tretinoin 0.01%/Fluocinolone acetonide 0.01%), a) 0.5 FL OZ (15 mL), b) 2 FL OZ (60 mL) bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600
Reason for Recall
Lack of Processing Controls (lack of assurance of conformity to specifications).
Distribution Pattern
Nationwide in the U.S.
Code Information
01-17-2020:45@4, 01-13-2020:40@27, BUD 7/7/2020 01-21-2020:43@11, BUD 7/18/2020 01-28-2020:88@15, 01-31-2020:73@6, BUD 7/26/2020 02-12-2020:43@16, 02-17-2020:86@5, BUD 8/10/2020 02-21-2020:23@1, BUD 8/16/2020
Source
- Dataset
- openFDA drug recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for D-1424-2020
- openFDA file date
- Nov 3, 2026
- Loaded by RegDataLab
- Nov 4, 2026