Independent register of U.S. FDA drug recalls · updated Oct 14, 2026
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FDA Drug Recalls

14,806 recalls, newest first

Class II · Moderate risk

0.2% Ropivacaine HCI

Lack of assurance of sterility: Three lots were released where there was a failure to follow proper testing and investigation procedures. Product may be out of specification (OOS) for endotoxin.

Terminated Sterility / contamination PharMEDium Services, LLC D-0423-2018
Class III · Low risk

Azelastine HCl Nasal Solution

Sun Pharmaceutical is recalling Azelastine HCl Nasal Solution, 0.1% (30 mL Bottle) following a failure to meet the % RSD requirement in the test for Droplet Size during the 6 month long term stability test station

Terminated Stability / shelf life Sun Pharmaceutical Industries, Inc. NDC 47335-779-91 D-0417-2018
Class III · Low risk

Klonopin (clonazepam)

Labeling: Not Elsewhere Classified: Schedule IV controlled substance indicator of CIV being omitted from the product carton, primary label is correct.

Terminated Labeling / mix-up Genentech, Inc. NDC 0004-0068-01 D-0416-2018
Class II · Moderate risk

VELCADE (bortezomib)

Defective Container: Confirmed reports of loose vial crimps.

Terminated Packaging defect Millennium Pharmaceuticals Inc. NDC 63020-0049-01 D-0425-2018
Class III · Low risk

Fentanyl Transdermal System

Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO) degradant exceeding the specification limits

Terminated Impurity / degradation Teva Pharmaceuticals USA NDC 0591-3214-72 D-0543-2018
Class III · Low risk

Fentanyl Transdermal System

Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO) degradant exceeding the specification limits

Terminated Impurity / degradation Teva Pharmaceuticals USA NDC 0591-3212-72 D-0541-2018
Class III · Low risk

Atorvastatin Calcium Tablets 40 mg

Failed Impurities/Degradations Specifications; out-of-specification results observed for Total Degradation Impurities during stability

Terminated Impurity / degradation Dr. Reddy's Laboratories, Inc. NDC 55111-123-05 D-0420-2018
Class III · Low risk

Atorvastatin Calcium Tablets 20 mg

Failed Impurities/Degradations Specifications; out-of-specification results observed for Total Degradation Impurities during stability

Terminated Impurity / degradation Dr. Reddy's Laboratories, Inc. NDC 55111-122-05 D-0419-2018
Class III · Low risk

Atorvastatin Calcium Tablets 10 mg

Failed Impurities/Degradations Specifications; out-of-specification results observed for Total Degradation Impurities during stability

Terminated Impurity / degradation Dr. Reddy's Laboratories, Inc. NDC 55111-121-05 D-0418-2018
Class I · High risk

Limbrel500

Marketed Without An Approved NDA/ANDA: Based on the labeling claims, these products are unapproved drugs for which the safety and efficacy have not been established and, therefore, subject to recall.

Terminated Unapproved drug Primus Pharmaceuticals, Inc. NDC 68040-606-16 D-0347-2018
Class I · High risk

Limbrel250

Marketed Without An Approved NDA/ANDA: Based on the labeling claims, these products are unapproved drugs for which the safety and efficacy have not been established and, therefore, subject to recall.

Terminated Unapproved drug Primus Pharmaceuticals, Inc. NDC 68040-605-16 D-0346-2018
Class I · High risk

Limbrel (flavocoxid 500 mg)

Marketed Without An Approved NDA/ANDA: Based on the labeling claims, these products are unapproved drugs for which the safety and efficacy have not been established and, therefore, subject to recall.

Terminated Unapproved drug Primus Pharmaceuticals, Inc. NDC 68040-602-16 D-0345-2018
Class I · High risk

Limbrel (flavocoxid 250 mg)

Marketed Without An Approved NDA/ANDA: Based on the labeling claims, these products are unapproved drugs for which the safety and efficacy have not been established and, therefore, subject to recall.

Terminated Unapproved drug Primus Pharmaceuticals, Inc. NDC 68040-601-16 D-0344-2018
Class III · Low risk

Cefuroxime

Subpotent Drug: The product is sub-potent prior to its 90-day beyond use date.

Terminated Wrong potency / content JCB Laboratories LLC D-0246-2018
Class III · Low risk

Ultane (sevoflurane)

Defective container: presence of a hole in the liners of the caps covering the product bottle, introducing possibility of leakage.

Terminated Packaging defect AbbVie Inc. NDC 0074-4456-51 D-0412-2018
Class III · Low risk

Oxycodone Hydrochloride Tablets

Labeling; Label Error Not Elsewhere Classified; label missing controlled substance CII symbol

Terminated Labeling / mix-up Ascent Pharmaceuticals, Inc. NDC 31722-917-01 D-0248-2018

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