Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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FDA Drug Recalls

708 recalls · Class II, newest first

Class II · Moderate risk

Dermamycin

CGMP Deviations: These products have been found to be misbranded as unapproved new drugs

Terminated Unapproved drug Herbal Doctor Remedies D-1116-2020
Class II · Moderate risk

De-Fibroidin

CGMP Deviations: These products have been found to be misbranded as unapproved new drugs

Terminated Unapproved drug Herbal Doctor Remedies D-1115-2020
Class II · Moderate risk

Cellulite Off

CGMP Deviations: These products have been found to be misbranded as unapproved new drugs

Terminated Unapproved drug Herbal Doctor Remedies D-1114-2020
Class II · Moderate risk

Blood Clot Purger

CGMP Deviations: These products have been found to be misbranded as unapproved new drugs

Terminated Unapproved drug Herbal Doctor Remedies D-1113-2020
Class II · Moderate risk

Bleeding Stop

CGMP Deviations: These products have been found to be misbranded as unapproved new drugs

Terminated Unapproved drug Herbal Doctor Remedies D-1112-2020
Class II · Moderate risk

Asthma Chest Rub

CGMP Deviations: These products have been found to be misbranded as unapproved new drugs

Terminated Unapproved drug Herbal Doctor Remedies D-1111-2020
Class II · Moderate risk

Asma Stopper

CGMP Deviations: These products have been found to be misbranded as unapproved new drugs

Terminated Unapproved drug Herbal Doctor Remedies D-1110-2020
Class II · Moderate risk

Age Stop Ex

CGMP Deviations: These products have been found to be misbranded as unapproved new drugs

Terminated Unapproved drug Herbal Doctor Remedies D-1109-2020
Class II · Moderate risk

Age Back

CGMP Deviations: These products have been found to be misbranded as unapproved new drugs

Terminated Unapproved drug Herbal Doctor Remedies D-1108-2020
Class II · Moderate risk

Acne Off

CGMP Deviations: These products have been found to be misbranded as unapproved new drugs

Terminated Unapproved drug Herbal Doctor Remedies D-1107-2020
Class II · Moderate risk

Acne Cystic

CGMP Deviations: These products have been found to be misbranded as unapproved new drugs

Terminated Unapproved drug Herbal Doctor Remedies D-1106-2020
Class II · Moderate risk

Acupuncture

CGMP Deviations: These products have been found to be misbranded as unapproved new drugs

Terminated Unapproved drug Herbal Doctor Remedies D-1105-2020
Class II · Moderate risk

Nystatin Oral Suspension

SubPotent Drug: Low out-of-specification results for assay testing.

Terminated Wrong potency / content PAI Holdings, LLC. dba Pharmaceutical Associates Inc NDC 0121-0810-16 D-1060-2020
Class II · Moderate risk

Methotrexate

Lack of Assurance of Sterility; the media used to conduct post-compounding sterility testing for the Methotrexate product was expired.

Terminated Sterility / contamination Edge Pharma, LLC D-0226-2021
Class II · Moderate risk

Oxycodone and Acetaminophen Tablets

CGMP Deviations: Products were manufactured in a processing area in which water leakage was observed

Terminated Packaging defect Aurobindo Pharma USA Inc. NDC 13107-046-01 D-1237-2020
Class II · Moderate risk

Phentermine Hydrochloride Capsules

CGMP Deviations: Products were manufactured in a processing area in which water leakage was observed

Terminated Packaging defect Aurobindo Pharma USA Inc. NDC 13107-105-01 D-1236-2020
Class II · Moderate risk

Mirtazapine Tablets

CGMP Deviations: Products were manufactured in a processing area in which water leakage was observed

Terminated Packaging defect Aurobindo Pharma USA Inc. NDC 13107-031-34 D-1235-2020
Class II · Moderate risk

Simvastatin Tablets

CGMP Deviations: Products were manufactured in a processing area in which water leakage was observed

Terminated Packaging defect Aurobindo Pharma USA Inc. NDC 65862-053-90 D-1234-2020
Class II · Moderate risk

Gabapentin Capsules

CGMP Deviations: Products were manufactured in a processing area in which water leakage was observed

Terminated Packaging defect Aurobindo Pharma USA Inc. NDC 65862-198-99 D-1232-2020

Recalls by year