US Drug Recall Register

FDA Drug Recalls

11,815 recalls · Class II, newest first

Class II · Moderate risk Terminated

Accuretic

Reason CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide impurity above the acceptable daily intake limit.

Pfizer Inc. NDC 0071-5212-23 D-0761-2022
Class II · Moderate risk Terminated

quinapril HCl/hydrochlorothiazide tablets

Reason CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide impurity above the acceptable daily intake limit.

Pfizer Inc. NDC 59762-0223-1 D-0760-2022
Class II · Moderate risk Terminated

quinapril HCl/hydrochlorothiazide tablets

Reason CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide impurity above the acceptable daily intake limit.

Pfizer Inc. NDC 59762-0220-1 D-0759-2022
Class II · Moderate risk Terminated

quinapril and hydrochlorothiazide tablets

Reason CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide impurity above the acceptable daily intake limit.

Pfizer Inc. NDC 59762-5225-9 D-0758-2022
Class II · Moderate risk Terminated

Accuretic

Reason CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide impurity above the acceptable daily intake limit.

Pfizer Inc. NDC 0071-0223-23 D-0757-2022
Class II · Moderate risk Terminated

Accuretic

Reason CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide impurity above the acceptable daily intake limit.

Pfizer Inc. NDC 0071-0220-23 D-0756-2022
Class II · Moderate risk Terminated

Accuretic

Reason CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide impurity above the acceptable daily intake limit.

Pfizer Inc. NDC 0071-0222-23 D-0755-2022
Class II · Moderate risk Terminated

Accuretic

Reason CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide impurity above the acceptable daily intake limit.

Pfizer Inc. NDC 0071-3112-23 D-0754-2022
Class II · Moderate risk Terminated

The Natural Dentist Healthy Breath Antiseptic Rinse

Reason Labeling; Label mix-up and Wrong Bar Code; back label incorrectly states active ingredient as Peppermint Oil and Sage Oil and has the wrong UPC

Revive Personal Products Company D-0751-2022
Class II · Moderate risk Terminated

Glycopyrrolate Tablets

Reason Presence of Foreign Substance: Complaint for pieces of glass discovered in a sealed bottle which came from equipment within the packaging room.

Aurolife Pharma, LLC NDC 13107-014-01 D-0736-2022
Class II · Moderate risk Terminated

Lidocaine Ointment USP

Reason cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.

Teligent Pharma, Inc. NDC 50383-341-35 D-0705-2022
Class II · Moderate risk Terminated

Lidocaine Cream 4%

Reason cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.

Teligent Pharma, Inc. NDC 0536-1281-28 D-0704-2022
Class II · Moderate risk Terminated

Hydrocortisone Butyrate Lotion

Reason cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.

Teligent Pharma, Inc. NDC 70512-032-04 D-0703-2022
Class II · Moderate risk Terminated

Gentamicin Sulfate Cream USP

Reason cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.

Teligent Pharma, Inc. NDC 70512-036-30 D-0702-2022
Class II · Moderate risk Terminated

Diflorasone Diacetate Ointment USP

Reason cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.

Teligent Pharma, Inc. NDC 52565-063-60 D-0701-2022
Class II · Moderate risk Terminated

Clobetasol Propionate Cream USP

Reason cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.

Teligent Pharma, Inc. NDC 70512-028-60 D-0700-2022
Class II · Moderate risk Terminated

Triamcinolone Acetonide Ointment USP

Reason cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.

Teligent Pharma, Inc. NDC 52565-014-15 D-0699-2022
Class II · Moderate risk Terminated

Triamcinolone Acetonide Lotion USP

Reason cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.

Teligent Pharma, Inc. NDC 52565-010-59 D-0698-2022
Class II · Moderate risk Terminated

Triamcinolone Acetonide Cream USP

Reason cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.

Teligent Pharma, Inc. NDC 52565-056-15 D-0697-2022
Class II · Moderate risk Terminated

Triamcinolone Acetonide Ointment USP

Reason cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.

Teligent Pharma, Inc. NDC 52565-048-15 D-0696-2022
Class II · Moderate risk Terminated

Nystatin and Triamcinolone Acetonide Ointment

Reason cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.

Teligent Pharma, Inc. NDC 52565-042-15 D-0695-2022
Class II · Moderate risk Terminated

Lidocaine Ointment USP

Reason cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.

Teligent Pharma, Inc. NDC 52565-008-14 D-0694-2022
Class II · Moderate risk Terminated

Lidocaine Cream

Reason cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.

Teligent Pharma, Inc. NDC 52565-122-15 D-0693-2022
Class II · Moderate risk Terminated

Hydrocortisone Butyrate Lotion

Reason cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.

Teligent Pharma, Inc. NDC 52565-087-02 D-0692-2022