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

Doxycycline

Labeling: Incorrect Or Missing Lot and/or Exp Date: Some expiries and lot numbers are missing.

Terminated Labeling / mix-up Galderma Laboratories, L.P. D-1031-2016
Class III · Low risk

Mycophenolate Mofetil

cGMP deviation; manufacturer is Not Registered with the Food and Drug Administration

Terminated cGMP deviation Attix Pharmaceuticals Inc D-1047-2016
Class III · Low risk

Dicloxacillin Sodium Capsules

Failed Impurities/Degradation Specifications:Out of specification result for a known impurity obtained during testing.

Terminated Impurity / degradation Sandoz, Inc NDC 0781-2248-01 D-1045-2016
Class III · Low risk

Hectorol (doxercalciferol injection)

Labeling: Wrong barcode. An incorrect bar code was noted on the vial label of Hectorol 2 mcg/1mL vial.

Terminated Labeling / mix-up Genzyme Corporation / Genzyme Biosurgery NDC 58468-0126-1 D-1029-2016
Class III · Low risk

CVS pharmacy Original Strength Acid Controller tablets

Failed impurities/degradation specification: An out of specification results has been determined for an individual related substance during stability testing at the 18th month interval for the Famotidine 10 mg Tablet, USP.

Terminated Impurity / degradation Dr. Reddy's Laboratories, Inc. D-1058-2016
Class III · Low risk

SKY Aspirin Chewable Tablets

Labeling: Label mix-up -outer carton incorrectly labeled as aspirin chewable tablets.

Terminated Labeling / mix-up Mckesson Packaging Services NDC 63739-434-01 D-0834-2016
Class III · Low risk

Haloperidol Decanoate Injection

Failed Impurities/Degradation Specifications: Firm is recalling product due to an impurity out-of-specification result.

Terminated Impurity / degradation Fresenius Kabi USA, LLC NDC 63323-469-01 D-0818-2016
Class III · Low risk

Lisinopril Tablets USP

CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.

Terminated Failed specification Lupin Pharmaceuticals Inc. NDC 68180-517-03 D-1503-2016
Class III · Low risk

Lisinopril Tablets USP

CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.

Terminated Failed specification Lupin Pharmaceuticals Inc. NDC 68180-516-02 D-1502-2016

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