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

362 recalls · Class III, newest first

Class III · Low risk

treatNOW ABILIFY

Labeling Not Elsewhere Classified: Physician sample kits/cartons of treatNOW Abilify are mislabeled. Product name is misspelled, storage instructions are missing and contents of kits may be incorrectly labeled on the outer packaging of the co-packaged kit.

Terminated Labeling / mix-up Otsuka Pharmaceutical Development & Commercialization, Inc. D-0018-2019
Class III · Low risk

treatNOW ABILIFY

Labeling Not Elsewhere Classified: Physician sample kits/cartons of treatNOW Abilify are mislabeled. Product name is misspelled, storage instructions are missing and contents of kits may be incorrectly labeled on the outer packaging of the co-packaged kit.

Terminated Labeling / mix-up Otsuka Pharmaceutical Development & Commercialization, Inc. D-0017-2019
Class III · Low risk

Oxycodone and Acetaminophen Tablets

Labeling: Incorrect or Missing Lot and/or Exp Date: Lot FG10517 is mislabeled on the primary container with Lot FG01517, shipper labels and invoices contain the correct lot number of FG10517.

Terminated Labeling / mix-up Mayne Pharma Inc NDC 68308-841-01 D-1129-2018
Class III · Low risk

Testosterone 200 mg Pellet

Labeling: Incorrect or Missing Lot and/or Exp Date: Incorrect expiration date on label

Terminated Labeling / mix-up Right Value Drug Stores, Inc. D-1047-2018
Class III · Low risk

Diazepam Rectal Gel

Labeling: Incorrect or Missing Lot and/or Exp Date: Product distributed without a lot number or expiration date on the outer carton.

Terminated Labeling / mix-up Valeant Pharmaceuticals North America LLC NDC 68682-650-20 D-1041-2018
Class III · Low risk

Equate ClearLAX

Labeling: Not Elsewhere Classified - A private label distributor noted unfiled NDC numbers on EQ ClearLax Polyethylene Glycol 3350 NF Powder Solution of various sizes.

Terminated Labeling / mix-up Lupin Somerset NDC 49035-312-07 D-0907-2018
Class III · Low risk

Riomet (metformin hydrochloride oral solution)

Labeling: Not Elsewhere Classified: Sun Pharma has decided to initiate this recall in response to identified labeling discrepancies in the patient literature.

Terminated Labeling / mix-up Sun Pharmaceutical Industries, Inc. NDC 10631-206-02 D-0818-2018
Class III · Low risk

Calendula Cream

Labeling: Labeling Error on Declared Strength; The outer carton (secondary packaging) statement of ingredients misstates the concentration of active ingredient at 7%. The primary packaging (tube) correctly states the active ingredient at 10%.

Terminated Labeling / mix-up Boiron Inc. D-0803-2018
Class III · Low risk

Indomethacin Capsules USP

Labeling: Incorrect Instructions: bottles incorrectly labeled with the usual adult dosage of "One or two capsules 2 or 3 times a day." rather than the correct usual adult dosage of "One capsule 2 or 3 times a day.

Terminated Labeling / mix-up Glenmark Pharmaceuticals Inc., USA NDC 68462-302-01 D-0606-2018
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 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
Class III · Low risk

Enoxaparin Sodium

Labeling: Label Error on Declared Strength. A single syringe labeled as 150 mg/1.0 mL was found packaged in a blister labeled as 120 mg/mL

Terminated Labeling / mix-up Sanofi-Aventis U.S. LLC NDC 0955-1012-10 D-0153-2018
Class III · Low risk

Clofarabine injection

Labeling: Incorrect or Missing Package Insert: authorized generic product was packaged with the incorrect insert for the brand name product Clolar (clofarabine) injection.

Terminated Labeling / mix-up Sanofi-Aventis U.S. LLC NDC 0955-1746-01 D-0056-2018

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