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

966 recalls · Class II, newest first

Class II · Moderate risk

Lactulose Solution

Microbial Contamination of Non-Sterile Products: bulk solution tested positive for the presence of the bacteria, Burkholderia cepacia.

Terminated Microbial contamination VistaPharm, Inc. NDC 66689-039-01 D-0146-2017
Class II · Moderate risk

L-Cysteine Hydrochloride Injection

Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing firm raised concerns that the product sterility may be compromised.

Terminated Sterility / contamination Sandoz Inc NDC 66758-005-01 D-0141-2017
Class II · Moderate risk

L-Cysteine Hydrochloride Injection

Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing firm raised concerns that the product sterility may be compromised.

Terminated Sterility / contamination Sandoz Inc NDC 66758-004-01 D-0140-2017
Class II · Moderate risk

Papa/Phen/Prost

Lack of Assurance of Sterility: product produced on a day there was an excursion in environmental monitoring data.

Terminated Sterility / contamination Fallon Wellness Pharmacy, L.L.C. D-0174-2017
Class II · Moderate risk

Papa/Phen/Prost

Lack of Assurance of Sterility: product produced on a day there was an excursion in environmental monitoring data.

Terminated Sterility / contamination Fallon Wellness Pharmacy, L.L.C. D-0173-2017
Class II · Moderate risk

Metformin Hydrochloride Tablets

Presence of Foreign Tablets/Capsules; report of Amlodipine Tablets found in 1000 count bottles of Metformin Hydrochloride Tablets USP

Terminated Particulate / foreign matter Ascend Laboratories LLC NDC 67877-217-10 D-0163-2017
Class II · Moderate risk

Salsalate Tablets

CGMP Deviations: manufactured under practices which may result in assay or content uniformity failures.

Terminated Wrong potency / content Nationwide Laboratories, LLC NDC 42937-704-10 D-0166-2017
Class II · Moderate risk

Salsalate Tablets

CGMP Deviations: manufactured under practices which may result in assay or content uniformity failures.

Terminated Wrong potency / content Nationwide Laboratories, LLC NDC 42937-703-18 D-0165-2017
Class II · Moderate risk

Urolet Mb Urinary Antiseptic

CGMP Deviations; deficiencies at the manufacturer may result in assay or content uniformity failures

Terminated Wrong potency / content Burel Pharmaceuticals Inc NDC 35573-302-30 D-0156-2017

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