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

D-Biotin 300 mg Capsule

Lack of Processing Controls (lack of assurance of conformity to specifications).

Terminated cGMP deviation MasterPharm LLC D-1419-2020
Class II · Moderate risk

Lidothol Patch

CGMP Deviations: Contract Manufacturing Organization (CMO) misplaced/lost batch records and test results for the recalled batch.

Terminated cGMP deviation Preferred Pharmaceuticals, Inc. D-1390-2020
Class II · Moderate risk

Carbamazepine 200 mg Tablets

FAILED DISSOLUTION SPECIFICATION: Low out-of-specification (OOS) dissolution results obtained during routine stability testing.

Terminated Dissolution failure RemedyRepack Inc. NDC 70518-2489-00 D-1387-2020
Class II · Moderate risk

Childrens Dimetapp Cold & Cough

Defective Delivery System: the dosing cups are missing graduations applicable to certain age groups.

Terminated Packaging defect Glaxosmithkline Consumer Healthcare Holdings D-1362-2020
Class II · Moderate risk

Heparin Sodium 5

Subpotent Drug: Out-of-Specification potency results at the 30-day stability timepoint.

Terminated Wrong potency / content SCA Pharmaceuticals NDC 70004-0650-46 D-1311-2020
Class II · Moderate risk

Tropical Lip Moisturizer

Superpotent Drug: The beginning portion of the batch appears to be approximately 25% superpotent for active ingredient Meradimate.

Terminated Wrong potency / content Yusef Manufacturing Laboratories, LLC D-1486-2020
Class II · Moderate risk

Clozapine Tablets USP tablet

Presence of foreign tablet: Consumer complaint of Clozapine Tablets 50mg being present in 500 count bottles of Clozapine Tablets USP 100mg.

Terminated Particulate / foreign matter Aurobindo Pharma USA Inc. NDC 65862-846-05 D-1370-2020
Class II · Moderate risk

Koala Hand Sanitizer

Subpotent Drug: active ingredient ethanol tested below label claim and there is presence of undeclared isopropyl alcohol.

Terminated Wrong potency / content Beaming White Llc D-1359-2020
Class II · Moderate risk

Koala Hand Sanitizer

Subpotent Drug: active ingredient ethanol tested below label claim and there is presence of undeclared isopropyl alcohol.

Terminated Wrong potency / content Beaming White Llc D-1358-2020
Class II · Moderate risk

Koala Hand Sanitizer

Subpotent Drug: active ingredient ethanol tested below label claim and there is presence of undeclared isopropyl alcohol.

Terminated Wrong potency / content Beaming White Llc D-1357-2020
Class II · Moderate risk

Irinotecan HCL Injection

Defective Container: Customer complaints received of a crimp defect while removing the flip-cap during use.

Terminated Packaging defect Hikma Pharmaceuticals USA Inc. NDC 0143-9583-01 D-1309-2020
Class II · Moderate risk

Irinotecan HCL Injection

Defective Container: Customer complaints received of a crimp defect while removing the flip-cap during use.

Terminated Packaging defect Hikma Pharmaceuticals USA Inc. NDC 0143-9701-01 D-1308-2020
Class II · Moderate risk

Aripiprazole Tablets

Labeling: Label mix up: Bottles labeled as aripiprazole 2 mg, 30 count had aripiprazole 5 mg tablets, 100 count.

Terminated Labeling / mix-up Alembic Pharmaceuticals Limited NDC 62332-097-30 D-1341-2020
Class II · Moderate risk

Nystatin Cream

Subpotent Drug: Out of specification for assay at the 9-month interval for Nystatin Cream, USP.

Terminated Wrong potency / content Crown Laboratories NDC 0316-0221-15 D-1339-2020
Class II · Moderate risk

Nystatin Cream

Subpotent Drug: Out of specification for assay at the 9-month interval for Nystatin Cream, USP.

Terminated Wrong potency / content Crown Laboratories NDC 0316-0221-30 D-1338-2020
Class II · Moderate risk

Time-Cap Labs

CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level

Terminated Nitrosamine impurity Marksans Pharma Limited NDC 49483-623-01 D-1356-2020
Class II · Moderate risk

metFORMIN HCL ER 500 mg

CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level

Terminated Nitrosamine impurity PD-Rx Pharmaceuticals, Inc. NDC 72789-009-30 D-1333-2020

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