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FDA Drug Recalls

Every FDA drug enforcement recall Public Health Trace has on record, republished from openFDA's official drug enforcement database. See Health Alerts for current, active recalls alongside outbreaks and advisories.

Drug recall information is sourced from the FDA's structured openFDA Enforcement Reports. Newly announced recalls may appear on FDA.gov before they become available in the structured dataset. See Methodology for how Public Health Trace imports and refreshes this data.

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Showing 5,981–6,000 of 17,964 drug recalls

Drug Recall Terminated Historical recordClass II

Progesterone Modified Release 100 mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600

by MasterPharm LLC

Reason
Lack of Processing Controls (lack of assurance of conformity to specifications).
Recall initiated
July 2, 2020
Reported by FDA
August 5, 2020
Distribution
Nationwide in the U.S.

View recall →

Drug Recall Terminated Historical recordClass II

Progesterone 50 mg Modified Release Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600

by MasterPharm LLC

Reason
Lack of Processing Controls (lack of assurance of conformity to specifications).
Recall initiated
July 2, 2020
Reported by FDA
August 5, 2020
Distribution
Nationwide in the U.S.

View recall →

Drug Recall Terminated Historical recordClass II

Progesterone 200 mg Troche, 30 troches per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600

by MasterPharm LLC

Reason
Lack of Processing Controls (lack of assurance of conformity to specifications).
Recall initiated
July 2, 2020
Reported by FDA
August 5, 2020
Distribution
Nationwide in the U.S.

View recall →

Drug Recall Terminated Historical recordClass II

Progesterone (Rapid-Dissolve) 150 mg Tablet, 30 tablets per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600

by MasterPharm LLC

Reason
Lack of Processing Controls (lack of assurance of conformity to specifications).
Recall initiated
July 2, 2020
Reported by FDA
August 5, 2020
Distribution
Nationwide in the U.S.

View recall →

Drug Recall Terminated Historical recordClass II

Progesterone 300 mg Troche, 30 troches per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600

by MasterPharm LLC

Reason
Lack of Processing Controls (lack of assurance of conformity to specifications).
Recall initiated
July 2, 2020
Reported by FDA
August 5, 2020
Distribution
Nationwide in the U.S.

View recall →

Drug Recall Terminated Historical recordClass II

Progesterone 150 mg Troche, 30 troches MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600

by MasterPharm LLC

Reason
Lack of Processing Controls (lack of assurance of conformity to specifications).
Recall initiated
July 2, 2020
Reported by FDA
August 5, 2020
Distribution
Nationwide in the U.S.

View recall →

Drug Recall Terminated Historical recordClass II

Progesterone (Modified Release) 150 mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600

by MasterPharm LLC

Reason
Lack of Processing Controls (lack of assurance of conformity to specifications).
Recall initiated
July 2, 2020
Reported by FDA
August 5, 2020
Distribution
Nationwide in the U.S.

View recall →

Drug Recall Terminated Historical recordClass II

Minoxidil/Biotin/Spironolactone 1.25/5/25mg capsules, 90 capsules per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600

by MasterPharm LLC

Reason
Lack of Processing Controls (lack of assurance of conformity to specifications).
Recall initiated
July 2, 2020
Reported by FDA
August 5, 2020
Distribution
Nationwide in the U.S.

View recall →

Drug Recall Terminated Historical recordClass II

Minoxidil/Biotin 1.25mg/5mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600

by MasterPharm LLC

Reason
Lack of Processing Controls (lack of assurance of conformity to specifications).
Recall initiated
July 2, 2020
Reported by FDA
August 5, 2020
Distribution
Nationwide in the U.S.

View recall →

Drug Recall Terminated Historical recordClass II

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

by MasterPharm LLC

Reason
Lack of Processing Controls (lack of assurance of conformity to specifications).
Recall initiated
July 2, 2020
Reported by FDA
August 5, 2020
Distribution
Nationwide in the U.S.

View recall →

Drug Recall Terminated Historical recordClass II

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.

by MasterPharm LLC

Reason
Lack of Processing Controls (lack of assurance of conformity to specifications).
Recall initiated
July 2, 2020
Reported by FDA
August 5, 2020
Distribution
Nationwide in the U.S.

View recall →

Drug Recall Terminated Historical recordClass II

Finasteride Plus 1.25mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600

by MasterPharm LLC

Reason
Lack of Processing Controls (lack of assurance of conformity to specifications).
Recall initiated
July 2, 2020
Reported by FDA
August 5, 2020
Distribution
Nationwide in the U.S.

View recall →

Drug Recall Terminated Historical recordClass II

Estriol 8 mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600

by MasterPharm LLC

Reason
Lack of Processing Controls (lack of assurance of conformity to specifications).
Recall initiated
July 2, 2020
Reported by FDA
August 5, 2020
Distribution
Nationwide in the U.S.

View recall →

Drug Recall Terminated Historical recordClass II

Estriol 6 mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600

by MasterPharm LLC

Reason
Lack of Processing Controls (lack of assurance of conformity to specifications).
Recall initiated
July 2, 2020
Reported by FDA
August 5, 2020
Distribution
Nationwide in the U.S.

View recall →

Drug Recall Terminated Historical recordClass II

D-Biotin 300 mg Capsule, 90 capsules per bottle, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600

by MasterPharm LLC

Reason
Lack of Processing Controls (lack of assurance of conformity to specifications).
Recall initiated
July 2, 2020
Reported by FDA
August 5, 2020
Distribution
Nationwide in the U.S.

View recall →

Drug Recall Terminated Historical recordClass II

Calcium citrate tetrahydrate USP powder, 100 gm container, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419, (866) 630-5600

by MasterPharm LLC

Reason
Lack of Processing Controls (lack of assurance of conformity to specifications).
Recall initiated
July 2, 2020
Reported by FDA
August 5, 2020
Distribution
Nationwide in the U.S.

View recall →

Drug Recall Terminated Historical recordClass II

Lisinopril Tablets USP, 10 mg, 1000 count bottles, Manufactured by: Lupin Limited, Nagpur INDIA, For BluePoint Laboratories NDC 68001-334-08

by Lupin Pharmaceuticals Inc.

Reason
Presence of Foreign Tablets/Capsules: Lisinopril Tablets USP, 20mg found in a 1000 count bottle of Lisinopril Tablets USP, 10mg
Recall initiated
July 17, 2020
Reported by FDA
August 5, 2020
Distribution
Product was distributed to OH and may have been further distributed throughout the United States.

View recall →

Drug Recall Terminated Historical recordClass II

Saniderm ADVANCED HAND SANITIZER, 70% Alcohol Content, 1 Liter bottles, Distributed by Polarized, LLC, Produced by Eskbiochem SA de CV, Mexico Japon 50, Celaya, Gto., Mexico, 38010. UPC 8 60003 63391 5.

by POLARIZED LLC

Reason
CGMP Deviations: Product was found to be below the label claim for ethanol content and the presence of undeclared methanol.
Recall initiated
June 25, 2020
Reported by FDA
August 5, 2020
Distribution
Distributed in VA with potential for Nationwide distribution in USA

View recall →

Drug Recall Terminated Historical recordClass II

Handese Advanced Instant Hand Sanitizer (Ethyl Alcohol 70%), 12 FL OZ (354 mL) bottles, www.handeseclean.com UPC 612520481094

by WORLD EVENT PROMOTIONS, LLC

Reason
Subpotent Drug: Product was found to be subpotent. Product also has high pH levels
Recall initiated
June 1, 2020
Reported by FDA
August 5, 2020
Distribution
Nationwide within the United States

View recall →

Drug Recall Terminated Historical recordClass III

Skin Medica Acne System, Contains: Purifying Foaming Wash (Salicylic Acid 2.0%), 5 fl oz.; Purifying Toner (Salicylic Acid 2.0%), 6 fl oz,; Acne Treatment Lotion (Benzoyl Peroxide 2.5%), 2 fl oz., Distributed in the U.S.A. by Allergan, Irvine, CA 92612, UPC 300234966005

by Allergan PLC

Reason
SUBPOTENT DRUG: Products failed assay results at the 12 and 24 month timepoints.
Recall initiated
July 6, 2020
Reported by FDA
August 5, 2020
Distribution
Nationwide within the United States

View recall →

Data last updated:

This information is republished from FDA's Recall Enterprise System through openFDA. Public Health Trace does not verify or supplement it, is not affiliated with the FDA, and does not provide medical advice -- always follow the guidance of your pharmacist, physician, or the recalling company for any medication you take. Read the full medical disclaimer.