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

1,586 recalls · Class II, newest first

Class II · Moderate risk

fentaNYL 400 mcg/200 mL

Presence of Particulate matter: manufacturer recalled fentanyl API due to potential for glass particules

Terminated Particulate / foreign matter QuVa Pharma, Inc. NDC 70092-1440-76 D-0554-2020
Class II · Moderate risk

fentaNYL 500 mcg/250 mL

Presence of Particulate matter: manufacturer recalled fentanyl API due to potential for glass particules

Terminated Particulate / foreign matter QuVa Pharma, Inc. NDC 70092-1225-37 D-0552-2020
Class II · Moderate risk

fentaNYL 1500 mcg/30 mL

Presence of Particulate matter: manufacturer recalled fentanyl API due to potential for glass particules

Terminated Particulate / foreign matter QuVa Pharma, Inc. NDC 70092-1099-49 D-0551-2020
Class II · Moderate risk

fentaNYL 200 mcg/100 mL

Presence of Particulate matter: manufacturer recalled fentanyl API due to potential for glass particules

Terminated Particulate / foreign matter QuVa Pharma, Inc. NDC 70092-1104-36 D-0550-2020
Class II · Moderate risk

fentaNYL 500 mcg/250 mL

Presence of Particulate matter: manufacturer recalled fentanyl API due to potential for glass particules

Terminated Particulate / foreign matter QuVa Pharma, Inc. NDC 70092-1269-37 D-0549-2020
Class II · Moderate risk

fentaNYL 200 mcg/100 mL

Presence of Particulate matter: manufacturer recalled fentanyl API due to potential for glass particules

Terminated Particulate / foreign matter QuVa Pharma, Inc. NDC 70092-1259-75 D-0548-2020
Class II · Moderate risk

fentaNYL 500 mcg/250 mL

Presence of Particulate matter: manufacturer recalled fentanyl API due to potential for glass particules

Terminated Particulate / foreign matter QuVa Pharma, Inc. NDC 70092-1105-37 D-0547-2020
Class II · Moderate risk

fentaNYL 500 mcg/250 mL

Presence of Particulate matter: manufacturer recalled fentanyl API due to potential for glass particules

Terminated Particulate / foreign matter QuVa Pharma, Inc. NDC 70092-1160-37 D-0546-2020
Class II · Moderate risk

Budesonide 0.4mg

Lack of Processing Controls

Terminated cGMP deviation Integrated Health Concepts Inc. dba Conversio Health D-0508-2020
Class II · Moderate risk

R2103

CGMP Deviations: products were not manufactured under current good manufacturing practices.

Terminated cGMP deviation Washington Homeopathic Products, Inc. D-0506-2020
Class II · Moderate risk

StellaLife VEGA Oral Gel Rinse

CGMP Deviations: products were not manufactured under current good manufacturing practices.

Terminated cGMP deviation Washington Homeopathic Products, Inc. D-0505-2020
Class II · Moderate risk

Pareira (Brava)

CGMP Deviations: products were not manufactured under current good manufacturing practices.

Terminated cGMP deviation Washington Homeopathic Products, Inc. D-0504-2020
Class II · Moderate risk

Silicea 6X Tablets

CGMP Deviations: products were not manufactured under current good manufacturing practices.

Terminated cGMP deviation Washington Homeopathic Products, Inc. D-0503-2020
Class II · Moderate risk

Natrum Sulphuricum 6X Tablets

CGMP Deviations: products were not manufactured under current good manufacturing practices.

Terminated cGMP deviation Washington Homeopathic Products, Inc. D-0502-2020

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