US Drug Recall Register

FDA Drug Recalls

14,801 recalls, newest first

Class III · Low risk Terminated

Enalapril Maleate

Reason Out-of-specification results for the Enalapril Diketopiperazine degradation product during commercial stability.

Aidarex Pharmaceuticals LLC D-0991-2018
Class III · Low risk Terminated

Enalapril Maleate

Reason Out-of-specification results for the Enalapril Diketopiperazine degradation product during commercial stability.

Aidarex Pharmaceuticals LLC D-0990-2018
Class I · High risk Terminated

Blissful Remedies Kratom+CBD CBD infused Maeng Da

Reason Microbial Contamination of Non-Sterile Products: The firm is initiating a recall of some of its products due to the potential of high microbial loads.

World Organix, LLC D-1126-2018
Class I · High risk Terminated

Blissful Remedies Gold Series Ultra Enhanced Indo

Reason Microbial Contamination of Non-Sterile Products: The firm is initiating a recall of some of its products due to the potential of high microbial loads.

World Organix, LLC D-1125-2018
Class I · High risk Terminated

Blissful Remedies

Reason Microbial Contamination of Non-Sterile Products: The firm is initiating a recall of some of its products due to the potential of high microbial loads.

World Organix, LLC D-1123-2018
Class I · High risk Terminated

Blissful Remedies Red Maeng Da

Reason Microbial Contamination of Non-Sterile Products: The firm is initiating a recall of some of its products due to the potential of high microbial loads.

World Organix, LLC D-1122-2018
Class III · Low risk Terminated

Enalapril Maleate Tablets

Reason Failed Impurities/Degradation Specifications: Sub-recall because this repackaged product was recalled by the manufacturing firm, Wockhardt, due to out-of-specification results for the Enalapril DiKetopiperazine degradation product.

Major Pharmaceuticals NDC 0904-5502-61 D-0980-2018
Class III · Low risk Terminated

Enalapril Maleate Tablets

Reason Failed Impurities/Degradation Specifications: Sub-recall because this repackaged product was recalled by the manufacturing firm, Wockhardt, due to out-of-specification results for the Enalapril DiKetopiperazine degradation product.

Major Pharmaceuticals NDC 0904-5609-61 D-0979-2018
Class II · Moderate risk Terminated

Glutathione 200mg/mL Injection w/Pres.

Reason Lack of Processing Controls: products produced in a manner that calls into question the sterility of the drug product intended to be sterile.

La Vita Compounding Pharmacy, LLC D-0923-2018
Class II · Moderate risk Terminated

Methyl Folate CA+ 1mg/ml Injection w/Pres.

Reason Lack of Processing Controls: products produced in a manner that calls into question the sterility of the drug product intended to be sterile.

La Vita Compounding Pharmacy, LLC D-0922-2018
Class II · Moderate risk Terminated

Methylcobalamin 1mg/mL Injection w/Pres.

Reason Lack of Processing Controls: products produced in a manner that calls into question the sterility of the drug product intended to be sterile.

La Vita Compounding Pharmacy, LLC D-0921-2018
Class III · Low risk Terminated

Enalapril Maleate Tablets USP

Reason Failed Impurities/Degradation Specification; out-of-specification results for the Enalapril DKT degradant

American Health Packaging NDC 68084-390-01 D-0915-2018
Class I · High risk Terminated

Gaia Kratom

Reason Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella contamination

Gaia Ethnobotanical LLC D-1016-2018
Class I · High risk Terminated

Gaia Kratom

Reason Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella contamination

Gaia Ethnobotanical LLC D-1015-2018
Class I · High risk Terminated

Gaia Kratom

Reason Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella contamination

Gaia Ethnobotanical LLC D-1014-2018
Class I · High risk Terminated

Gaia Kratom

Reason Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella contamination

Gaia Ethnobotanical LLC D-1013-2018
Class I · High risk Terminated

Gaia Kratom

Reason Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella contamination

Gaia Ethnobotanical LLC D-1012-2018
Class I · High risk Terminated

Gaia Kratom

Reason Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella contamination

Gaia Ethnobotanical LLC D-1011-2018
Class I · High risk Terminated

Gaia Kratom

Reason Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella contamination

Gaia Ethnobotanical LLC D-1010-2018
Class I · High risk Terminated

Gaia Kratom

Reason Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella contamination

Gaia Ethnobotanical LLC D-1009-2018
Class I · High risk Terminated

Gaia Kratom

Reason Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella contamination

Gaia Ethnobotanical LLC D-1008-2018
Class I · High risk Terminated

Gaia Kratom

Reason Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella contamination

Gaia Ethnobotanical LLC D-1007-2018