Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class III drug recalls - low risk

Class III means the product is unlikely to cause harm but violates FDA labeling or manufacturing rules. These are the recalls you rarely hear about; pharmacies usually just swap the affected lot.

1,716 recalls, newest first.

Class III · Low risk

Gabapentin Tablets

Presence of Foreign Tablets/Capsules: Pharmacist reported presence of some Gabapentin tablets 800 mg comingled in Gabapentin 600 mg 500 count bottles.

Terminated Particulate / foreign matter Sciegen Pharmaceuticals Inc D-0354-2023
Class III · Low risk

Buprenorphine Transdermal System

Failed Impurities/Degradation Specifications: Out of specification for related substance 10-hydroxy buprenorphine N-Oxide results generated at the 18-month stability timepoint.

Terminated Impurity / degradation AVEVA Drug Delivery Systems, Inc. NDC 60505-7079-05 D-0466-2023
Class III · Low risk

Buprenorphine Transdermal System

Failed Impurities/Degradation Specifications: Out of specification for related substance 10-hydroxy buprenorphine N-Oxide results generated at the 18-month stability timepoint.

Terminated Impurity / degradation AVEVA Drug Delivery Systems, Inc. NDC 60505-7077-05 D-0465-2023
Class III · Low risk

Bd-102 Nf

Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.

Terminated Impurity / degradation DuPont Nutrition USA, Inc D-0352-2023
Class III · Low risk

Avicel PH-200 NF

Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.

Terminated Impurity / degradation DuPont Nutrition USA, Inc D-0351-2023
Class III · Low risk

Avicel PH- 102 NF

Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.

Terminated Impurity / degradation DuPont Nutrition USA, Inc D-0350-2023
Class III · Low risk

Avicel PH- 101 NF

Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.

Terminated Impurity / degradation DuPont Nutrition USA, Inc D-0349-2023
Class III · Low risk

Levofloxacin Tablets

Mismatching of the embossing on the tablets (T7) with the embossing mentioned in the package insert (ML63) in the distributed bottles.

Terminated Labeling / mix-up Macleods Pharma USA, INC NDC 33342-022-08 D-0162-2023
Class III · Low risk

SINUVA (mometasone furoate)

Failed Dissolution Specification; product did not meet the average 24-hour drug release rate (dissolution) specification stability time point at 9 months.

Terminated Dissolution failure Intersect ENT, Inc. NDC 10599-003-01 D-0167-2023
Class III · Low risk

Timolol Maleate Ophthalmic Solution

Failed Stability Specifications: Out of specification for weight loss at the 18-month stability timepoint and projected weight loss of 21.1% at shelf life.

Terminated Stability / shelf life Apotex Corp. NDC 60505-1005-4 D-0093-2023
Class III · Low risk

Lacosamide Oral Solution

Failed Excipient Specifications: out of specification result observed for p-Hydroxybenzoic Acid content

Terminated Failed specification Camber Pharmaceuticals, Inc NDC 31722-627-26 D-0094-2023
Class III · Low risk

Allergy Relief D

Failed dissolution specifications

Terminated Dissolution failure Dr. Reddy's Laboratories, Inc. NDC 49032-273-20 D-0073-2023
Class III · Low risk

Phenytoin Sodium Injection

Labeling: Not elsewhere classified; the product is being recalled because of customer complaints that the primary vial label was missing a barcode.

Terminated Labeling / mix-up Acella Pharmaceuticals, LLC NDC 42192-614-05 D-0070-2023
Class III · Low risk

Phenytoin Sodium Injection

Labeling: Not elsewhere classified; the product is being recalled because of customer complaints that the primary vial label was missing a barcode.

Terminated Labeling / mix-up Acella Pharmaceuticals, LLC NDC 42192-614-02 D-0069-2023
Class III · Low risk

Susvimo (ranibizumab injection)

Defective Delivery System: Commercial implants do not meet the filed specification for the intended use, a few patients have experienced an issue with the implants that renders it non-functioning.

Terminated Packaging defect Genentech Inc NDC 50242-078-55 D-0025-2023

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