US Drug Recall Register

FDA Drug Recalls

11,815 recalls · Class II, newest first

Class II · Moderate risk Terminated

Pulmicort Respules 0.5 mg/2mL s

Reason Lack of Processing Controls.

Kroger Specialty Pharmacy, Inc. NDC 00186-1989-04 D-0739-2018
Class II · Moderate risk Terminated

Polyethylene Glycol 3350

Reason Lack of Processing Controls.

Kroger Specialty Pharmacy, Inc. NDC 51991-0457-57 D-0738-2018
Class II · Moderate risk Terminated

Pediasure Liq. Vanilla G+G

Reason Lack of Processing Controls.

Kroger Specialty Pharmacy, Inc. NDC 70074-0558-98 D-0737-2018
Class II · Moderate risk Terminated

Kalydeco 150 mg tablet blister

Reason Lack of Processing Controls.

Kroger Specialty Pharmacy, Inc. NDC 51167-0200-01 D-0736-2018
Class II · Moderate risk Terminated

Humira Pen Sub-q Kit a.) 40 mg/0.8 mL

Reason Lack of Processing Controls.

Kroger Specialty Pharmacy, Inc. NDC 00074-4339-02 D-0734-2018
Class II · Moderate risk Terminated

WipeEssentials Wet Wipes

Reason CGMP Deviations: finished products were manufactured with poor quality water.

Diamond Wipes International, Inc. D-0630-2018
Class II · Moderate risk Terminated

Acure

Reason CGMP Deviations: finished products were manufactured with poor quality water.

Diamond Wipes International, Inc. D-0629-2018
Class II · Moderate risk Terminated

Amantadine HCl Capsules

Reason Failed Dissolution Specifications

AVKARE Inc. NDC 50268-069-15 D-0633-2018
Class II · Moderate risk Terminated

Zhong Hua Jiu

Reason CGMP Deviations: the product was produced with substandard GMP manufacturing processes.

United Pacific Co Ltd NDC 53614-001-02 D-0624-2018
Class II · Moderate risk Terminated

Conzerol

Reason cGMP Deviations

Elroselabs Inc. D-0623-2018
Class II · Moderate risk Terminated

Molleave

Reason cGMP Deviations

Elroselabs Inc. D-0622-2018
Class II · Moderate risk Terminated

Levofloxacin in 5% Dextrose Injection

Reason Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap

AuroMedics Pharma LLC NDC 55150-245-52 D-0709-2018
Class II · Moderate risk Terminated

Levofloxacin in 5% Dextrose Injection

Reason Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap

AuroMedics Pharma LLC NDC 55150-244-47 D-0708-2018
Class II · Moderate risk Terminated

Levetiracetam in 0.54% Sodium Chloride Injection

Reason Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap

AuroMedics Pharma LLC NDC 55150-248-47 D-0707-2018
Class II · Moderate risk Terminated

Levetiracetam in 0.75% Sodium Chloride Injection

Reason Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap

AuroMedics Pharma LLC NDC 55150-247-47 D-0706-2018
Class II · Moderate risk Terminated

Levetiracetam in 0.82% Sodium Chloride Injection

Reason Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap

AuroMedics Pharma LLC NDC 55150-246-47 D-0705-2018
Class II · Moderate risk Terminated

Levofloxacin in 5% Dextrose Injection

Reason Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap

AuroMedics Pharma LLC NDC 55150-243-46 D-0704-2018