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

1,293 recalls, newest first

Class III · Low risk

Virt-Nate Prenatal/Postnatal

Tablets/Capsules Imprinted with Wrong ID; product debossed with an incorrect punch. Bottles could contain tablets debossed with V259 (debossing for PreTab) instead of the correct punch, V264 (debossing for Virt-Nate).

Terminated Labeling / mix-up Virtus Pharmaceuticals, Llc D-0775-2016
Class III · Low risk

NABUMETONE Tablets USP

Labeling: Not Elsewhere Classified: Lack of leaflets and approved labels on bottles.

Terminated Labeling / mix-up Teva Pharmaceuticals USA D-0773-2016
Class II · Moderate risk

Rocuronium Bromide 50 MG/5ML INJ.

Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.

Terminated Labeling / mix-up RemedyRepack Inc. NDC 61786-0222-57 D-0517-2016
Class II · Moderate risk

Novolin 70/30

Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.

Terminated Labeling / mix-up RemedyRepack Inc. NDC 52125-0414-01 D-0516-2016
Class II · Moderate risk

Lorazepam 2 mg/mL Inj.

Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.

Terminated Labeling / mix-up RemedyRepack Inc. NDC 61786-0316-01 D-0515-2016
Class II · Moderate risk

Ascorbic Acid 500 MG/ML Inj.

Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.

Terminated Labeling / mix-up RemedyRepack Inc. NDC 61786-0431-16 D-0514-2016
Class II · Moderate risk

Vitamin B-Complex 100

Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.

Terminated Labeling / mix-up RemedyRepack Inc. NDC 52125-0873-02 D-0513-2016
Class II · Moderate risk

Bicillin L-A 600000 Units/mL Inj.

Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.

Terminated Labeling / mix-up RemedyRepack Inc. NDC 61786-0253-03 D-0512-2016
Class II · Moderate risk

Humulin 70/30

Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.

Terminated Labeling / mix-up RemedyRepack Inc. NDC 52125-0415-08 D-0511-2016
Class III · Low risk

Prednisone 20 mg

Labeling: Not elsewhere classified. NDC number is incorrect on the container.

Terminated Labeling / mix-up Northwind Pharmaceuticals LLC NDC 51655-320-53 D-0485-2016
Class II · Moderate risk

Kindest Kare Antimicrobial Foaming Handwash

Labeling: Not Elsewhere Classified; Incorrect/Undeclared Excipients: Outdated previous version of label applied to products that incorrectly states one inactive ingredient.

Terminated Labeling / mix-up Steris Corp NDC 0519-1452-13 D-0518-2016
Class III · Low risk

Donnatal

Labeling: Not elsewhere classified - Product label incorrectly lists Scopolamine Hydrocodone as an active ingredient on the side panel instead of Scopolamine Hydrobromide.

Terminated Labeling / mix-up Rx PAK NDC 59212-425-10 D-0053-2016
Class II · Moderate risk

WellPatch¿ Capsaicin Pain Relief Patch

Labeling: Incorrect Instructions; The word not is missing from the following sentences "do bandage tightly or cover with any type of wrap except clothing and "do use with a heating pad or with other heat sources in the Drug Facts panel "Warning" section

Terminated Labeling / mix-up The Mentholatum Co. NDC 10742-8126-2 D-0018-2016
Class III · Low risk

Lamivudine Oral Solution

Labeling: Incorrect or Missing Lot and/or Exp. Date - Firm received a customer complaint that the expiration date printed on the unit carton (5/18) does not match the expiration date on the bottle label (5/17).

Terminated Labeling / mix-up Silarx Pharmaceutical, Inc. NDC 54838-0566-70 D-1416-2015
Class III · Low risk

Ampicillin Capsules

Labeling: Incorrect Or Missing Package Insert: Product is labeled with unapproved labeling.

Terminated Labeling / mix-up Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals D-1350-2015
Class III · Low risk

Desmopressin Acetate Tablets

Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted with an X on one side.

Terminated Labeling / mix-up American Health Packaging D-1235-2015

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