RecallRadar

FDA Drug recall D-1423-2020

Formula 82F (Minoxidil 5%/Tretinoin 0.01%/Fluocinolone Acetonide 0.01%/Finasteride 0.25%), 0.5 FL OZ (15 mL) bottle MasterPharm, 115-02 Lib…

On 2020-08-05 the FDA classified a Class II recall of Formula 82F (Minoxidil 5%/Tretinoin 0.01%/Fluocinolone Acetonide 0.01%/Finasteride 0.25%), 0.5 FL OZ (15 mL) bottle MasterPharm, 115-02 Lib… by Masterpharm, citing lack of Processing Controls (lack of assurance of conformity to specifications).

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1423-2020
ClassificationClass II
Statusterminated
Initiated2020-07-02
Published2020-08-05
Last updated2026-09-13 11:52 UTC
CompanyMasterpharm
DistributionUS

Product

Formula 82F (Minoxidil 5%/Tretinoin 0.01%/Fluocinolone Acetonide 0.01%/Finasteride 0.25%), 0.5 FL OZ (15 mL) bottle MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600.

Reason

Lack of Processing Controls (lack of assurance of conformity to specifications).

Identifiers

code_info01-15-2020:70@3, 01-09-2020:48@2, BUD 7/7/2020 01-20-2020:79@11, 01-23-2020:55@11, BUD 7/18/2020 01-29-2020:18@1, 02-03-2020:89@8, BUD 7/26/2020

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1423-2020%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.