Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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FDA Drug Recalls

943 recalls · Class II, newest first

Class II · Moderate risk

Human Chorionic Gonadotropin 5

Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD) exceed the BUD/EXP of at least one ingredient used to make final product.

Terminated Labeling / mix-up KRS Global Biotechnology, Inc D-0175-2018
Class II · Moderate risk

Human Chorionic Gonadotropin 2

Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD) exceed the BUD/EXP of at least one ingredient used to make final product.

Terminated Labeling / mix-up KRS Global Biotechnology, Inc D-0174-2018
Class II · Moderate risk

Estriol 0.1%

Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD) exceed the BUD/EXP of at least one ingredient used to make final product.

Terminated Labeling / mix-up KRS Global Biotechnology, Inc D-0172-2018
Class II · Moderate risk

Bi-Est (Estriol/Estradiol)

Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD) exceed the BUD/EXP of at least one ingredient used to make final product.

Terminated Labeling / mix-up KRS Global Biotechnology, Inc D-0168-2018
Class II · Moderate risk

Benzocaine 20%

Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD) exceed the BUD/EXP of at least one ingredient used to make final product.

Terminated Labeling / mix-up KRS Global Biotechnology, Inc D-0166-2018
Class II · Moderate risk

Benzocaine 20%

Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD) exceed the BUD/EXP of at least one ingredient used to make final product.

Terminated Labeling / mix-up KRS Global Biotechnology, Inc D-0165-2018
Class II · Moderate risk

Anastrozole SR 1 mg Capsules

Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD) exceed the BUD/EXP of at least one ingredient used to make final product.

Terminated Labeling / mix-up KRS Global Biotechnology, Inc D-0163-2018
Class II · Moderate risk

Anastrozole 0.5 mg Capsules

Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD) exceed the BUD/EXP of at least one ingredient used to make final product.

Terminated Labeling / mix-up KRS Global Biotechnology, Inc D-0161-2018
Class II · Moderate risk

Succinylcholine 20 MG/ML INJ

Labeling: Incorrect or Missing Lot and/or Exp Date; incorrect expiration date on the labeling of the outer poly bag

Terminated Labeling / mix-up Ace Surgical Supply Co., Inc. D-0071-2018
Class II · Moderate risk

Lorazepam Tablets

Labeling: Label Error on Declared Strength. Bottle labeled as 0.5 mg tablets contained 1mg tablets of lorazepam

Terminated Labeling / mix-up Leading Pharma, LLC NDC 69315-904-05 D-0085-2018
Class II · Moderate risk

ChloraPrep OneStep

Labeling; Label Mixup; the immediate package is labeled incorrectly as Chloroprep Onestep (Clear), however, the correct label should be Chloroprep with Tint (Hi Lite Orange)

Terminated Labeling / mix-up Becton Dickinson & Company D-0029-2018
Class II · Moderate risk

Aminocaproic Acid

CGMP Deviations: Product manufactured for Industrial Use but was labeled and distributed for Pharmacy Compounding Use.

Terminated Labeling / mix-up Medisca, Inc. NDC 38779-0989-05 D-1174-2017
Class II · Moderate risk

Acarbose Tablets

Labeling: Incorrect or Missing Lot and/or Exp Date: An incorrect expiration date of July 2018 is printed on the product labeling rather than the correct expiration date of July 2017.

Terminated Labeling / mix-up Teva Pharmaceuticals USA NDC 16252-523-01 D-1178-2017
Class II · Moderate risk

Povidone Iodine

Labeling: Label mix-up. Finished product Povidone iodine 7.5% was labeled as Povidone iodine 10% , the outer box had the correct label.

Terminated Labeling / mix-up Degasa Sa De Cv NDC 68345-350-09 D-1129-2017
Class II · Moderate risk

Vitamin A&D Ointment

Labeling Mixup; the individual A&D ointment foil packets are incorrectly labeled as petroleum jelly. The boxes and outer case are correctly labeled as A&D ointment.

Terminated Labeling / mix-up Medline Industries INC D-1138-2017
Class II · Moderate risk

Carbamazepine Oral Suspension

Labeling Error: Label mix-up. Products' unit dose cups are correctly labeled, but the product carton lists incorrect volume and NDC.

Terminated Labeling / mix-up Precision Dose Inc. NDC 68094-301-59 D-1037-2017
Class II · Moderate risk

Cyclobenzaprine HCl Tablets

Labeling; Label Mix up; cartons labeled as Amantadine HCl 100 mg Capsules contain unit dose blister cards of Cyclobenzaprine HCl Tablet, USP 5 mg

Terminated Labeling / mix-up Apace KY LLC D-1036-2017
Class II · Moderate risk

Amantadine HCl Capsules

Labeling; Label Mix up; cartons labeled as Amantadine HCl 100 mg Capsules contain unit dose blister cards of Cyclobenzaprine HCl Tablet, USP 5 mg

Terminated Labeling / mix-up Apace KY LLC D-1035-2017

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