Independent register of U.S. FDA drug recalls · updated Oct 13, 2026
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FDA Drug Recalls

11,818 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
Class II · Moderate risk

Duloxetine Delayed-release Capsules USP 30 mg 30-count bottles

Failed Tablet/Capsule Specifications: Capsule shell (s) opening inside the bottle The Initial reports stated one or two capsules in a bottle count of 30s opening. First report came in June 14, 2016. Till date about 22 reports have come in from pharmacies which report two batches 130/16/001 and 130/16/002. Third batch 130/16/003 is not distributed yet, will be recalled from warehouse.

Terminated Failed specification Inventia Healthcare Private Limited NDC 69097-298-02 D-0224-2017
Class II · Moderate risk

Succinylcholine Chloride

Lack of Assurance of Sterility: A portion of the batch quantity was compounded outside of the firm's process media validation.

Terminated Sterility / contamination Pharmedium Services, LLC NDC 61553-0364-65 D-0125-2017
Class II · Moderate risk

DIPYRIDAMOLE Tablets USP

Presence of foreign tablets/capsules: 50 mg Persantine tablets were found in a 75 mg Persantine 100-count bottle and 50 mg Persantine tablet was found in a 100 count bottle of 75 mg Dipyridamole.

Terminated Particulate / foreign matter Boehringer Ingelheim Pharmaceuticals, Inc. NDC 0054-0436-25 D-0114-2017
Class II · Moderate risk

Persantine

Presence of foreign tablets/capsules: 50 mg Persantine tablets were found in a 75 mg Persantine 100-count bottle and 50 mg Persantine tablet was found in a 100 count bottle of 75 mg Dipyridamole.

Terminated Particulate / foreign matter Boehringer Ingelheim Pharmaceuticals, Inc. NDC 0597-0019-01 D-0113-2017

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