Independent register of U.S. FDA drug recalls · updated Oct 13, 2026
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Class II drug recalls - moderate risk

Class II means the product may cause temporary or medically reversible harm, and serious harm is unlikely. It is by far the largest recall class - most potency, dissolution and labeling problems land here.

14,543 recalls, newest first.

Class II · Moderate risk

metformin HCL ER 500 mg

CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level (per manufacturer)

Terminated Nitrosamine impurity PD-Rx Pharmaceuticals, Inc. D-0059-2021
Class II · Moderate risk

Time-Cap Labs

CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level

Terminated Nitrosamine impurity Marksans Pharma Limited NDC 49483-624-01 D-0062-2021
Class II · Moderate risk

Time-Cap Labs

CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level

Terminated Nitrosamine impurity Marksans Pharma Limited NDC 49483-623-09 D-0061-2021
Class II · Moderate risk

SYP Health Hand Sanitizer Alcohol Gel

CGMP Deviations: product manufactured at the same facility that produced product that FDA sampled and found to be subpotent for ethanol and contained methanol.

Completed Chemical / undeclared Aa Products INC D-0102-2021
Class II · Moderate risk

Nature-Throid 1 GR

CGMP deviations; repackaged product was recalled by the manufacturer because it was manufactured under the same conditions as products found to be sub-potent.

Terminated cGMP deviation PD-Rx Pharmaceuticals, Inc. NDC 43063-819-01 D-0005-2021
Class II · Moderate risk

Phentermine

cMGP Deviations: Drug products repackaged into pouches without supporting stability studies.

Terminated Stability / shelf life Calvin Scott & Company, Inc. NDC 00527-0597-10 D-0011-2021
Class II · Moderate risk

Diethylpropion

cMGP Deviations: Drug products repackaged into pouches without supporting stability studies.

Terminated Stability / shelf life Calvin Scott & Company, Inc. NDC 00527-1477-01 D-0010-2021
Class II · Moderate risk

Diethylpropion

cMGP Deviations: Drug products repackaged into pouches without supporting stability studies.

Terminated Stability / shelf life Calvin Scott & Company, Inc. NDC 00527-1475-01 D-0009-2021
Class II · Moderate risk

Killz Germz Hand Sanitizer

Sub-Potent Drug; Killz GERMz was recalled due to sub-potent results. Testing revealed ethanol levels as low as 62% while labelled claim is 70%.

Ongoing Labeling / mix-up Genesis Partnership Company SA NDC 74625-003-05 D-0041-2021
Class II · Moderate risk

Killz Germz Hand Sanitizer

Sub-Potent Drug; Killz GERMz was recalled due to sub-potent results. Testing revealed ethanol levels as low as 62% while labelled claim is 70%.

Ongoing Labeling / mix-up Genesis Partnership Company SA NDC 74625-003-04 D-0040-2021
Class II · Moderate risk

Genesis Hand Sanitizer Gel

CGMP Deviations: hand sanitizers were recalled because they were manufactured in the same facility as another hand sanitizer product with sub-potent ethanol levels.

Ongoing cGMP deviation Genesis Partnership Company SA NDC 74484-002-04 D-0039-2021
Class II · Moderate risk

Genesis Hand Sanitizer Gel

CGMP Deviations: hand sanitizers were recalled because they were manufactured in the same facility as another hand sanitizer product with sub-potent ethanol levels.

Ongoing cGMP deviation Genesis Partnership Company SA NDC 74484-002-02 D-0038-2021
Class II · Moderate risk

Panagel Hand Sanitizer

CGMP Deviations: hand sanitizers were recalled because they were manufactured in the same facility as another hand sanitizer product with sub-potent ethanol levels.

Ongoing cGMP deviation Genesis Partnership Company SA NDC 78384-001-04 D-0037-2021

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