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

Losartan Potassium Tablets

CGMP Deviations: Impurity for N-nitroso-N-methyl-4-aminobutryric Acid (NBMA) detected in active ingredient (API) used to manufacture finished products.

Terminated Nitrosamine impurity Golden State Medical Supply Inc. NDC 60429-316-30 D-1238-2020
Class II · Moderate risk

Lisinopril Tablets USP

Presence of Foreign Tablet/ Capsule: Product complaint received indicating mix-up of one lisinopril 5mg tablet inside of a 30 mg, 100-count bottle of Lisinopril Tablets.

Terminated Particulate / foreign matter Lupin Pharmaceuticals Inc. NDC 68180-982-01 D-1079-2020
Class II · Moderate risk

Glycopyrrolate Tablets

Failed Impurities/Degradation Specification: Presence of unknown impurity observed.

Terminated Impurity / degradation Par Pharmaceutical Inc. NDC 49884-0065-01 D-1071-2020
Class II · Moderate risk

Losartan Potassium Tablets USP 100 mg

CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level

Terminated Nitrosamine impurity Avet Pharmaceuticals, Inc. NDC 23155-646-03 D-1104-2020
Class II · Moderate risk

Losartan Potassium Tablets USP 50 mg

CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level

Terminated Nitrosamine impurity Avet Pharmaceuticals, Inc. NDC 23155-645-03 D-1103-2020
Class II · Moderate risk

Losartan Potassium Tablets

CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.

Ongoing Nitrosamine impurity Teva Pharmaceuticals USA NDC 0591-3747-00 D-1102-2020
Class II · Moderate risk

Losartan Potassium Tablets

CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.

Ongoing Nitrosamine impurity Teva Pharmaceuticals USA NDC 0591-3746-00 D-1101-2020
Class II · Moderate risk

Losartan Potassium Tablets

CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.

Ongoing Nitrosamine impurity Teva Pharmaceuticals USA NDC 0591-3745-00 D-1100-2020
Class II · Moderate risk

Thyro-H

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

Terminated Unapproved drug Herbal Doctor Remedies D-1174-2020
Class II · Moderate risk

BioMycin

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

Terminated Unapproved drug Herbal Doctor Remedies D-1173-2020
Class II · Moderate risk

Worm Off

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

Terminated Unapproved drug Herbal Doctor Remedies D-1172-2020
Class II · Moderate risk

Voice Rescue

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

Terminated Unapproved drug Herbal Doctor Remedies D-1171-2020
Class II · Moderate risk

Vitiligo Off Ointment

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

Terminated Unapproved drug Herbal Doctor Remedies D-1170-2020
Class II · Moderate risk

Vigo-XXX

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

Terminated Unapproved drug Herbal Doctor Remedies D-1169-2020
Class II · Moderate risk

Vertigo Off

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

Terminated Unapproved drug Herbal Doctor Remedies D-1168-2020
Class II · Moderate risk

Tution 130

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

Terminated Unapproved drug Herbal Doctor Remedies D-1167-2020

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