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

170 recalls · Class III, newest first

Class III · Low risk

Acetic Acid Otic Solution

Subpotent Drug: The product/lot is out-of-specification (OOS) for the assay of acetic acid at the 18-month test station.

Terminated Wrong potency / content Hi-Tech Pharmacal Co., Inc. NDC 50383-889-15 D-302-2013
Class III · Low risk

Nupercainal

Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or expiration date may be illegible.

Terminated Labeling / mix-up Novartis Consumer Health NDC 0067-5812-96 D-208-2013
Class III · Low risk

Myoflex (trolamine salicylate)

Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or expiration date may be illegible.

Terminated Labeling / mix-up Novartis Consumer Health D-207-2013
Class III · Low risk

Voltaren 1% Gel

Labeling: Incorrect or Missing Lot and/or Expiration Date; This recall is being initiated because the lot number and expiration date on the tube may not be legible.

Terminated Labeling / mix-up Physicians Total Care, Inc. NDC 54868-5965-00 D-596-2013
Class III · Low risk

Fenofibric Acid

Labeling: Incorrect instructions; an error in section 5.11 of the patient insert that results in incorrect medical advice. Specifically, the labeling should read "If a severely depressed HDL-C level is detected, fibrate therapy should be withdrawn, and the HDL-C level monitored until it has returned to baseline, and fibrate therapy should not be re-initiated." The labeling for the recalled lots

Terminated Labeling / mix-up Mutual Pharmaceutical Company, Inc. NDC 53489-678-07 D-400-2014
Class III · Low risk

Fenofibric Acid

Labeling: Incorrect instructions; an error in section 5.11 of the patient insert that results in incorrect medical advice. Specifically, the labeling should read "If a severely depressed HDL-C level is detected, fibrate therapy should be withdrawn, and the HDL-C level monitored until it has returned to baseline, and fibrate therapy should not be re-initiated." The labeling for the recalled lots

Terminated Labeling / mix-up Mutual Pharmaceutical Company, Inc. NDC 53489-677-07 D-399-2014
Class III · Low risk

FIBRICOR (fenofibric acid)

Labeling: Incorrect instructions; an error in section 5.11 of the patient insert that results in incorrect medical advice. Specifically, the labeling should read "If a severely depressed HDL-C level is detected, fibrate therapy should be withdrawn, and the HDL-C level monitored until it has returned to baseline, and fibrate therapy should not be re-initiated." The labeling for the recalled lots

Terminated Labeling / mix-up Mutual Pharmaceutical Company, Inc. NDC 13310-102-07 D-398-2014
Class III · Low risk

Lisinopril Tablets

Tablets/Capsules Imprinted With Wrong ID: Pharmaceuticals are imprinted with an incorrect identifier code on the embossed tablets..

Terminated Labeling / mix-up Mylan Pharmaceuticals Inc. D-269-2013
Class III · Low risk

Ethambutol Hydrochloride Tablets USP

Failed Impurities/Degradation Specifications: This product is being recalled due to an out of specification result for an impurity.

Terminated Impurity / degradation Lupin Pharmaceuticals Inc. NDC 68180-281-01 D-346-2014
Class III · Low risk

Voltaren Gel

Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or Expiration date on the tube may not be legible in this lot.

Terminated Labeling / mix-up Novartis Consumer Health NDC 63481-684-83 D-577-2013
Class III · Low risk

Lamisil AT Cream

Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or Expiration date on the tube may not be legible in this lot.

Terminated Labeling / mix-up Novartis Consumer Health NDC 0067-6295-43 D-576-2013
Class III · Low risk

Novartis Lamisil AT Cream for Jock Itch

Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or Expiration date on the tube may not be legible in this lot.

Terminated Labeling / mix-up Novartis Consumer Health NDC 0067-3999-12 D-575-2013
Class III · Low risk

Target Up & Up

Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or Expiration date on the tube may not be legible in this lot..

Terminated Labeling / mix-up Novartis Consumer Health NDC 0067-6382-30 D-574-2013
Class III · Low risk

Novartis Lamisil AT Cream

Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or Expiration date on the tube may not be legible in this lot.

Terminated Labeling / mix-up Novartis Consumer Health D-573-2013
Class III · Low risk

Jevantique

Chemical contamination: Firm's inspection discovered the presence of 2-phenylphenol in the product due to migration from the cardboard cartons in which the product is packaged.

Terminated Chemical / undeclared Warner Chilcott Company LLC NDC 52544-237-19 D-304-2013

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