US Drug Recall Register

FDA Drug Recalls

17,898 recalls, newest first

Class II · Moderate risk Terminated

Levocarnitine 100mg/Ml Mdv Soln

Reason Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns

First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy D-0030-2022
Class II · Moderate risk Terminated

Magnesium Chloride

Reason Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns

First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy D-0029-2022
Class II · Moderate risk Terminated

Calcium Chloride

Reason Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns

First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy D-0028-2022
Class II · Moderate risk Terminated

Pi yen chin Ophthalmic Redness Reliever Drops Made in China

Reason Labeling: Not Elsewhere Classified; The packaging states these are ophthalmic drops. However, they are manufactured as nasal drops and sterility cannot be assured.

Anhui Welcome Foreign Trade Co.,ltd. NDC 51367-008-10 D-0755-2021
Class I · High risk Terminated

Hydro Pinapple Burn Max Health Thach Dua

Reason Marketed without an approved NDA/ ANDA - presence of undeclared sibutramine

Ebay Seller - John Nguyen D-0797-2021
Class II · Moderate risk Terminated

Carbamazepine 200mg Tablets

Reason Failed Dissolution Specifications

The Harvard Drug Group NDC 0904-6172-61 D-0807-2021
Class II · Moderate risk Terminated

Micafungin for Injection

Reason Labeling; Incorrect or Missing Package Insert: The package insert provided with the product does not include all required sections approved for this product. This includes aspects of Adverse Reactions, Drug Interactions and Use in Specific Populations.

Xellia Pharmaceuticals USA, LLC NDC 70594-037-01 D-0757-2021
Class II · Moderate risk Terminated

Micafungin for Injection

Reason Labeling; Incorrect or Missing Package Insert: The package insert provided with the product does not include all required sections approved for this product. This includes aspects of Adverse Reactions, Drug Interactions and Use in Specific Populations.

Xellia Pharmaceuticals USA, LLC NDC 70594-036-01 D-0756-2021
Class III · Low risk Terminated

Bleomycin for Injection

Reason Labeling: Not elsewhere classified: Mislabeling

Hikma Pharmaceuticals USA Inc. NDC 0143-9240-01 D-0771-2021
Class III · Low risk Terminated

Avicel

Reason Out of specification results for conductivity.

DuPont Nutrition USA, Inc D-0728-2021
Class II · Moderate risk Terminated

Fexofenadine Hydrochloride Tablets

Reason Failed Impurities/Degradation Specifications

The Harvard Drug Group NDC 0904-6979-40 D-0289-2022
Class II · Moderate risk Terminated

Clopidogrel Tablets

Reason Presence of foreign matter

Macleods Pharma Usa Inc NDC 33342-060-15 D-0787-2021
Class II · Moderate risk Terminated

Artificial Tears Ointment

Reason Non-Sterility - OOS sterility testing observed during 12-month controlled room temperature stability testing. The microbiological investigation identified the organism as a member of the Bacillus cereus group.

Akorn, Inc. NDC 17478-062-35 D-0786-2021
Class I · High risk Terminated

365 SKINNY High Intensity Capsules

Reason Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared sibutramine, a previously approved drug that was withdrawn from the US market due to safety concerns.

Je Dois Lavoir LLC D-0631-2022
Class II · Moderate risk Terminated

Fludarabine Phosphate for Injection

Reason Lack of Assurance of Sterility: the manufacturing firm had microbial recoveries during environmental monitoring in aseptic areas of manufacturing.

Custopharm, Inc. NDC 24201-237-01 D-0765-2021
Class II · Moderate risk Ongoing

Combipatch

Reason Failed Stability Specifications; out of specification for shear.

Noven Pharmaceuticals Inc NDC 68968-0525-2 D-0725-2021
Class II · Moderate risk Ongoing

Combipatch

Reason Failed Stability Specifications; out of specification for shear.

Noven Pharmaceuticals Inc NDC 68968-0514-2 D-0724-2021
Class II · Moderate risk Terminated

Succinylcholine Chloride 100 mg/5 mL

Reason Lack of sterility assurance

BayCare Integrated Service Center, LLC /dba BayCare Central Pharmacy D-0702-2021
Class II · Moderate risk Terminated

Entacapone Tablets

Reason Failed Dissolution Specifications

The Harvard Drug Group NDC 0904-6822-04 D-0806-2021
Class III · Low risk Terminated

Lidocaine Ointment USP

Reason Failed Viscosity Specifications: lot does not meet specification for Viscosity, which was determined through routine testing.

Teligent Pharma, Inc. NDC 52565-008-14 D-0785-2021
Class II · Moderate risk Terminated

Cyclobenzaprine Hydrochloride Tablets

Reason CGMP Deviations: Out of specification (OOS) test result for Total Aerobic Microbial Count (TAMC) and Total Yeast and Mold Count (TYMC) for an excipient batch of Dibasic Calcium Phosphate.

Teva Pharmaceuticals USA NDC 57237-266-01 D-0776-2021