FDA recall record

MasterPharm Formula 82M recall — FDA D-1424-2020

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

Class IIclassification
D-1424-2020official record ID
Aug 5, 2020report date

Recall record at a glance

Official recordD-1424-2020
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMasterPharm LLC
Report dateAug 5, 2020
Recall initiation dateJul 2, 2020
Quantity543 units
LocationSouth Richmond Hill, NY, United States

Official 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

Why the product was recalled

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

Distribution information

Nationwide in the U.S.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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