US Drug Recall Register

FDA Drug Recalls

11,815 recalls · Class II, newest first

Class II · Moderate risk Terminated

Levoxyl

Reason Superpotent

Pfizer Inc. NDC 60793-860-01 D-0150-2017
Class II · Moderate risk Terminated

Papa/Phen/Prost

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

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

Papa/Phen/Prost

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

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

Metformin Hydrochloride Tablets

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

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

Fentanyl Citrate Injection

Reason Lack of Assurance of Sterility: Complaints of broken tips on the ampules.

Hospira Inc. NDC 0409-4093-32 D-0153-2017
Class II · Moderate risk Terminated

Phenazopyridine Hydrochloride Tablets

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

Nationwide Laboratories, LLC NDC 42937-702-10 D-0168-2017
Class II · Moderate risk Terminated

Phenazopyridine Hydrochloride Tablets

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

Nationwide Laboratories, LLC NDC 42937-701-10 D-0167-2017
Class II · Moderate risk Terminated

Salsalate Tablets

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

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

Salsalate Tablets

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

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

Phenazopyridine Hydrochloride Tablets

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

Burel Pharmaceuticals Inc NDC 35573-306-10 D-0162-2017
Class II · Moderate risk Terminated

Phenazopyridine Hydrochloride Tablets

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

Burel Pharmaceuticals Inc NDC 35573-304-10 D-0161-2017
Class II · Moderate risk Terminated

Indiomin MB URINARY ANTISEPTIC

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

Burel Pharmaceuticals Inc NDC 35573-315-10 D-0160-2017
Class II · Moderate risk Terminated

AZUPHEN MB URINARY ANTISEPTIC Capsules

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

Burel Pharmaceuticals Inc NDC 35573-314-10 D-0159-2017
Class II · Moderate risk Terminated

UROPHEN MB URINARY ANTISEPTIC Tablets

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

Burel Pharmaceuticals Inc NDC 35573-307-10 D-0158-2017
Class II · Moderate risk Terminated

URAMIT MB URINARY ANTISEPTIC Capsules

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

Burel Pharmaceuticals Inc NDC 35573-300-10 D-0157-2017
Class II · Moderate risk Terminated

Urolet Mb Urinary Antiseptic

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

Burel Pharmaceuticals Inc NDC 35573-302-30 D-0156-2017
Class II · Moderate risk Terminated

Hyolev MB URINARY ANTISEPTIC Tablets

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

Burel Pharmaceuticals Inc NDC 35573-301-90 D-0155-2017
Class II · Moderate risk Terminated

Sodium Chloride Ophthalmic Solution

Reason Subpotent Drug: concentration of product is less than labeled amount.

Akorn Inc NDC 17478-623-12 D-0124-2017
Class II · Moderate risk Terminated

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

Reason 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.

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

Succinylcholine Chloride

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

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

DIPYRIDAMOLE Tablets USP

Reason 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.

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

Persantine

Reason 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.

Boehringer Ingelheim Pharmaceuticals, Inc. NDC 0597-0019-01 D-0113-2017
Class II · Moderate risk Terminated

Travoprost Ophthalmic Solution USP

Reason Lack of Assurance of Sterility; damage to the internal portion of the dropper tip portion of the container

Par Pharmaceutical, Inc. D-0154-2017
Class II · Moderate risk Terminated

Phenobarbital Tablets

Reason Failed Dissolution Specifications: Phenobarbital Tablets have an out of specification for dissolution at the 12 month stability time point

West-Ward Pharmaceuticals Corp. NDC 0143-1455-01 D-1045-2017
Class II · Moderate risk Terminated

PredniSONE Tablets USP

Reason Failed Tablet/Capsule Specifications: Discovery of an underweight tablet.

West-Ward Pharmaceutical NDC 0054-4741-25 D-0008-2017