US Drug Recall Register

FDA Drug Recalls

17,898 recalls, newest first

Class II · Moderate risk Terminated

Acetaminophen Oral Suspension

Reason cGMP Deviations: Product manufactured with contaminated raw ingredient.

Precision Dose Inc. D-0094-2022
Class III · Low risk Terminated

Clonidine Transdermal System

Reason Failed Impurities/Degradation Specifications

Teva Pharmaceuticals USA NDC 0591-3508-04 D-0235-2022
Class II · Moderate risk Terminated

Cartia XT

Reason Labelling: Incorrect Exp. Date

Teva Pharmaceuticals USA NDC 62037-597-90 D-0232-2022
Class II · Moderate risk Terminated

artnaturals Hand Sanitizer

Reason CGMP Deviations: Other lots recalled because they were manufactured using common ingredients as the contaminated lot

Virgin Scent INC D-0784-2022
Class II · Moderate risk Terminated

artnaturals hand sanitizer

Reason CGMP Deviations: Other lots recalled because they were manufactured using common ingredients as the contaminated lot

Virgin Scent INC D-0783-2022
Class I · High risk Terminated

artnaturals hand sanitizer

Reason Chemical Contamination: presence of benzene, acetaldehyde, and acetal.

Virgin Scent INC D-0782-2022
Class II · Moderate risk Terminated

Maximum Strength Nasal Spray

Reason CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.

Perrigo Company PLC NDC 41250-989-10 D-0629-2022
Class II · Moderate risk Terminated

Maximum Strength Nasal Spray

Reason CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.

Perrigo Company PLC NDC 41250-989-10 D-0628-2022
Class II · Moderate risk Terminated

Sinus Severe

Reason CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.

Perrigo Company PLC NDC 55910-696-10 D-0627-2022
Class II · Moderate risk Terminated

No Drip Nasal Spray

Reason CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.

Perrigo Company PLC NDC 49035-388-10 D-0626-2022
Class II · Moderate risk Terminated

No Drip Nasal Spray

Reason CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.

Perrigo Company PLC NDC 36800-388-10 D-0625-2022
Class II · Moderate risk Terminated

Maximum Strength No Drip Nasal Spray

Reason CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.

Perrigo Company PLC NDC 30142-388-10 D-0624-2022
Class II · Moderate risk Terminated

No Drip Nasal Spray

Reason CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.

Perrigo Company PLC NDC 41163-703-10 D-0623-2022
Class II · Moderate risk Terminated

No Drip Nasal Decongestant

Reason CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.

Perrigo Company PLC NDC 21130-801-10 D-0622-2022
Class II · Moderate risk Terminated

Maximum Strength No Drip Nasal Spray

Reason CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.

Perrigo Company PLC NDC 11822-6319-1 D-0621-2022
Class II · Moderate risk Terminated

Maximum Strength No Drip Nasal Spray

Reason CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.

Perrigo Company PLC NDC 30142-388-10 D-0620-2022
Class II · Moderate risk Terminated

Maximum Strength No Drip Nasal Spray

Reason CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.

Perrigo Company PLC NDC 41250-388-10 D-0619-2022
Class II · Moderate risk Terminated

Soothing 12 Hour Nasal Decongestant Spray No Drip

Reason CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.

Perrigo Company PLC NDC 0904-6761-30 D-0618-2022
Class II · Moderate risk Terminated

Nasal Spray Decongestant

Reason CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.

Perrigo Company PLC NDC 30142-388-10 D-0617-2022
Class II · Moderate risk Terminated

Maxiumum Strength No Drip Nasal Spray

Reason CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.

Perrigo Company PLC NDC 55910-623-10 D-0616-2022
Class II · Moderate risk Terminated

No Drip Nasal Mist

Reason CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.

Perrigo Company PLC NDC 59779-388-10 D-0615-2022
Class II · Moderate risk Terminated

Maximum Strength No Drip Nasal Spray

Reason CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.

Perrigo Company PLC NDC 72288-388-10 D-0614-2022
Class II · Moderate risk Terminated

Maximum Strength No Drip Nasal Spray

Reason CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.

Perrigo Company PLC NDC 72288-388-10 D-0613-2022
Class II · Moderate risk Terminated

Severe Congestion Nasal Spray

Reason CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.

Perrigo Company PLC NDC 36800-907-10 D-0612-2022