Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Manufacturing (cGMP) deviations

Departures from current Good Manufacturing Practice found in production or during FDA inspection. A broad quality-system cause: the batch was made under conditions that fall short of FDA manufacturing standards.

1,754 FDA drug recalls with this cause, newest first.

This category covers departures from current Good Manufacturing Practice during production. It is FDA's broadest label, used when a facility's own process control failed somewhere along the line even if no single ingredient was proven unsafe on its own. Where the report names a specific consequence - a temperature excursion, a contaminant, a potency problem - we file the recall under that more specific cause instead; what remains here is the genuinely general case.

Class II · Moderate risk

Integrity Biochem HSC70-LV

CGMP Deviation: Third party test results showing a presence of acetal and acetaldehyde at levels above USP specified amounts.

Terminated cGMP deviation Integrity Bio-Chemicals LLC D-0110-2024
Class II · Moderate risk

Integrity Biochem HSC 70-LM

CGMP Deviation: Third party test results showing a presence of acetal and acetaldehyde at levels above USP specified amounts.

Terminated cGMP deviation Integrity Bio-Chemicals LLC D-0109-2024
Class II · Moderate risk

Gynazole-1

Incorrect Product Formulation: Hydrophilic Colloidal Silica was used to manufacture the product rather than Hydrophobic Colloidal Silica as required by the manufacturing process.

Ongoing cGMP deviation Padagis US LLC D-0081-2024
Class II · Moderate risk

AstrinGyn (Ferric Subsulfate)

CGMP Deviations: Products not manufactured under current good manufacturing practices.

Completed cGMP deviation Ecometics, Inc. NDC 59365-6065-0 D-1101-2023
Class II · Moderate risk

activator concentrate

CGMP Deviations: Products not manufactured under current good manufacturing practices.

Completed cGMP deviation Ecometics, Inc. D-1100-2023
Class II · Moderate risk

Unguentine Ointment

CGMP Deviations: Products not manufactured under current good manufacturing practices.

Completed cGMP deviation Ecometics, Inc. D-1099-2023
Class II · Moderate risk

Alcolado Relampago

CGMP Deviations: Products not manufactured under current good manufacturing practices.

Completed cGMP deviation Ecometics, Inc. D-1098-2023
Class II · Moderate risk

Yager's Liniment

CGMP Deviations: Products not manufactured under current good manufacturing practices.

Completed cGMP deviation Ecometics, Inc. D-1097-2023
Class II · Moderate risk

Blis-To-Sol Liquid

CGMP Deviations: Products not manufactured under current good manufacturing practices.

Completed cGMP deviation Ecometics, Inc. D-1096-2023
Class II · Moderate risk

Rufinamide Tablets

cGMP deviations: Batch was released prior to approval.

Terminated cGMP deviation Aurobindo Pharma USA Inc. NDC 59651-617-08 D-1088-2023
Class II · Moderate risk

Rufinamide Tablets

cGMP deviations: Batch was released prior to approval.

Terminated cGMP deviation Aurobindo Pharma USA Inc. NDC 59651-616-08 D-1087-2023
Class II · Moderate risk

ROcuronium Bromide 50 mg/5 mL

CGMP Violations- that spaces adjacent to the production area may have been compromised at the time of production.

Terminated cGMP deviation New England Life Care, Inc. dba Advanced Compounding Solutions D-0928-2023