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

41 recalls, newest first

Class II · Moderate risk

Nystatin 150 Mu

Labeling: Label Error on Declared Strength: Assay value on the label is incorrect.

Ongoing Labeling / mix-up Fagron, Inc NDC 51552-0041-1 D-0157-2024
Class II · Moderate risk

Nystatin 2 Bu

Labeling: Label Error on Declared Strength: Assay value on the label is incorrect.

Ongoing Labeling / mix-up Fagron, Inc NDC 51552-0041-4 D-0156-2024
Class II · Moderate risk

Nystatin 500 Mu

Labeling: Label Error on Declared Strength: Assay value on the label is incorrect.

Ongoing Labeling / mix-up Fagron, Inc NDC 51552-0041-3 D-0155-2024
Class II · Moderate risk

Nystatin 5bu

Labeling: Label Error on Declared Strength: Assay value on the label is incorrect.

Ongoing Labeling / mix-up Fagron, Inc NDC 51552-0041-5 D-0154-2024
Class III · Low risk

Tropicamide 1%

Labeling: Label Mix-Up: The label of a dropper bottle mistakenly states the container is a 0.5mL single-use syringe instead of a 5 mL dropper

Ongoing Labeling / mix-up Fagron Compounding Services NDC 71266-8240-01 D-0125-2024
Class III · Low risk

LET Gel

Product Mix-up: Incorrect Product Formulation

Terminated Labeling / mix-up Right Value Drug Stores, LLC dba Carie Boyd's Prescription Shop NDC 73271-1003-1 D-0140-2024
Class II · Moderate risk

Naproxen Tablets

Labeling: Label Mix-Up-Indomethacin bottles may be labeled as Naproxen

Ongoing Labeling / mix-up Glenmark Pharmaceuticals Inc., USA NDC 68462-188-01 D-0124-2024
Class II · Moderate risk

Indomethacin 25mg Capsules

Labeling: Label Mix-Up-Indomethacin bottles may be labeled as Naproxen

Ongoing Labeling / mix-up Glenmark Pharmaceuticals Inc., USA NDC 68462-406-01 D-0123-2024
Class III · Low risk

Synthroid

Labeling: Wrong Barcode- One (1) of every forty (40) unit dose blister will contain incorrect barcode information that causes a 125mcg unit dose is scanned as 200mcg unit dose.

Ongoing Labeling / mix-up AbbVie Inc. NDC 0074-7068-11 D-0088-2024
Class III · Low risk

VANCOmycin HCI PF

Labeling: Not Elsewhere Classified

Terminated Labeling / mix-up Denver Solutions, LLC DBA Leiters Health NDC 71449-029-68 D-0072-2024
Class III · Low risk

VANCOmycin HCI PF

Labeling: Not Elsewhere Classified

Terminated Labeling / mix-up Denver Solutions, LLC DBA Leiters Health NDC 71449-028-68 D-0071-2024
Class III · Low risk

Oxytocin synthetic

Labeling: Not Elsewhere Classified

Terminated Labeling / mix-up Denver Solutions, LLC DBA Leiters Health NDC 71449-157-70 D-0070-2024
Class II · Moderate risk

Digoxin Tablets

Labeling: Label Mix-Up- Bottles labeled as Digoxin Tablets, USP 0.125 mg contain Digoxin Tablets, USP 0.25mg and bottles labeled as Digoxin Tablets, USP 0.25mg contain Digoxin Tablets, USP 0.125mg.

Terminated Labeling / mix-up Marlex Pharmaceuticals, Inc. NDC 10135-0748-01 D-1170-2023
Class I · High risk

Digoxin Tablets

Labeling: Label Mix-Up- Bottles labeled as Digoxin Tablets, USP 0.125 mg contain Digoxin Tablets, USP 0.25mg and bottles labeled as Digoxin Tablets, USP 0.25mg contain Digoxin Tablets, USP 0.125mg.

Terminated Labeling / mix-up Marlex Pharmaceuticals, Inc. NDC 10135-0747-01 D-1169-2023
Class III · Low risk

Bendamustine HCl Injection

Labeling: Missing Label; customer complaint received that labels were partially or completely peeled off injection vial.

Completed Labeling / mix-up Baxter Healthcare Corporation NDC 10019-079-01 D-1103-2023
Class II · Moderate risk

Capsaicin Cream 0.025%

Product mix-up: Cartons labeled Capsaicin Cream 0.025% may contain tubes of Sodium Fluoride 1.1% Prescription Dental Toothpaste

Terminated Labeling / mix-up Avkare LLC NDC 50268-195-60 D-1147-2023
Class II · Moderate risk

Sodium Fluoride 1.1%

Cases of Sodium Fluoride 1.1% Prescription Dental Toothpaste may contain cartons labeled as Capsaicin Cream 0.025% but contain correctly labeled tubes of Sodium Fluoride 1.1% Prescription Dental Toothpaste

Terminated Labeling / mix-up Avkare LLC NDC 42291-741-51 D-1146-2023
Class II · Moderate risk

hello wild strawberry fluoride toothpaste

Labeling: Label Mix-Up: Some hello wild strawberry fluoride toothpaste, packaged in cartons labeled as hello wild strawberry fluoride toothpaste were incorrectly filled in tubes labeled as hello fresh watermelon fluoride free toothpaste.

Terminated Labeling / mix-up Colgate Palmolive Company D-1084-2023
Class III · Low risk

Pluvicto 1

Labeling: Incorrect or Missing Lot and/or Exp Date: vials were labeled with the incorrect lot number and expiration date

Terminated Labeling / mix-up Advanced Accelerator Applications USA, Inc. NDC 69488-010-61 D-1085-2023
Class III · Low risk

0.9% Sodium Chloride Injection USP

Labeling: Not Elsewhere Classified - the description, warnings, storage information and instructions for use are either missing or partially printed.

Terminated Labeling / mix-up B. Braun Medical Inc. NDC 0264-5802-00 D-1083-2023
Class I · High risk

ZIPRASIDONE HYDROCHLORIDE CAPSULES 20 mg

Labeling: Label Mix-up: Unit Dose cartons labeled as Ziprasidone Hydrochloride Capsules, 20 mg were found to contain blister packages labeled as and containing Dronabinol Capsules, USP, 2.5 mg.

Terminated Labeling / mix-up The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories NDC 0904-6269-08 D-0893-2023
Class III · Low risk

Methylprednisolone Acetate Injectable Suspension

Labeling: Not Elsewhere Classified; A typographical error was observed in the NDC number on the preprinted Individual Folding Cartons (secondary packaging only). Incorrect NDC Number 70121-1573-1; Correct NDC Number 70121-1574-1.

Terminated Labeling / mix-up Amneal Pharmaceuticals of New York, LLC NDC 70121-1574-01 D-0756-2023

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