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

Dextroamphetamine Saccharate

Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule

Terminated Labeling / mix-up Amerisource Health Services NDC 60687-133-25 D-1483-2016
Class II · Moderate risk

Dextroamphetamine Saccharate

Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule

Terminated Labeling / mix-up Amerisource Health Services NDC 68084-936-25 D-1482-2016
Class II · Moderate risk

Dextroamphetamine Saccharate

Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule

Terminated Labeling / mix-up Amerisource Health Services NDC 68084-874-25 D-1481-2016
Class II · Moderate risk

Transderm Scop

Defective Delivery System; reports of damaged product that may alter the predicted release of scopolamine following transdermal application.

Terminated Packaging defect Sandoz Inc D-0133-2017
Class II · Moderate risk

DOBUTamine Injection

Discoloration: Firm received complaints of product discoloration and particulates.

Terminated Failed specification Hospira Inc. NDC 0409-2025-20 D-1500-2016
Class II · Moderate risk

Ephedrine Sulfate Injection

Lack of Assurance of Sterility: An FDA inspection at the facility raised concerns that product sterility was potentially impacted.

Terminated Sterility / contamination Allergy Laboratories, Inc. NDC 69053-008-02 D-1498-2016
Class II · Moderate risk

Senna Syrup

CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.

Terminated Microbial contamination Pharmatech LLC NDC 0904-6289-09 D-1526-2016
Class II · Moderate risk

Senexon Liquid

CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.

Terminated Microbial contamination Pharmatech LLC NDC 0536-1000-59 D-1525-2016
Class II · Moderate risk

Diocto Syrup

CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.

Terminated Microbial contamination Pharmatech LLC NDC 0536-1001-85 D-1524-2016
Class II · Moderate risk

Aller-Chlor

CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.

Terminated Microbial contamination Pharmatech LLC NDC 0536-1025-47 D-1523-2016
Class II · Moderate risk

Ninjacof-A

CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.

Terminated Microbial contamination Pharmatech LLC NDC 23359-033-16 D-1522-2016
Class II · Moderate risk

Sennazon (sennosides)

CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.

Terminated Microbial contamination Pharmatech LLC NDC 76518-100-08 D-1520-2016
Class II · Moderate risk

Zinc Acetate

Does not meet monograph: product exhibits lead levels in excess of the USP monograph limits.

Terminated Unapproved drug Spectrum Laboratory Products, Inc. D-1456-2016
Class II · Moderate risk

2% Chlorhexidine Gluconate* Cloth

CGMP Deviations: potential contamination of products manufactured on the same equipment and lines as the contaminated product.

Terminated cGMP deviation Sage Products LLC NDC 53462-705-20 D-0231-2017
Class II · Moderate risk

Comfort Shield

CGMP Deviations: potential contamination of products manufactured on the same equipment and lines as the contaminated product.

Terminated cGMP deviation Sage Products LLC NDC 53462-915-50 D-0230-2017

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