US Drug Recall Register

FDA Drug Recalls

1,523 recalls · Class III, newest first

Class III · Low risk Terminated

Klonopin

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

Genentech, Inc. NDC 0004-0068-01 D-0416-2018
Class III · Low risk Terminated

Metformin Hydrochloride Tablets

Reason Presence of Foreign Tablet: Metformin BP 1000mg was found in bottle of Metformin HCl 1000mg

Aurobindo Pharma Ltd. NDC 65862-010-05 D-0427-2018
Class III · Low risk Terminated

Norco

Reason Labeling: Not Elsewhere Classified: does not have the required "CII" controlled drug classification indication on the primary label.

Allergan NDC 0023-6022-01 D-0413-2018
Class III · Low risk Terminated

Fentanyl Transdermal System

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

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

Fentanyl Transdermal System. 75 mcg/h

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

Teva Pharmaceuticals USA NDC 0591-3213-72 D-0542-2018
Class III · Low risk Terminated

Fentanyl Transdermal System

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

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

Fentanyl Transdermal System. 25 mcg/h

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

Teva Pharmaceuticals USA NDC 0591-3198-72 D-0540-2018
Class III · Low risk Terminated

Atorvastatin Calcium Tablets 40 mg

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

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

Atorvastatin Calcium Tablets 20 mg

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

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

Atorvastatin Calcium Tablets 10 mg

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

Dr. Reddy's Laboratories, Inc. NDC 55111-121-05 D-0418-2018
Class III · Low risk Terminated

Megestrol Acetate Oral Suspension

Reason Subpotent Drug: Out of specification for assay (stability testing)

Mckesson Packaging Services NDC 63739-549-51 D-0338-2018
Class III · Low risk Terminated

Cefuroxime

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

JCB Laboratories LLC D-0246-2018
Class III · Low risk Terminated

Ultane

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

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

Oxycodone Hydrochloride Tablets

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

Ascent Pharmaceuticals, Inc. NDC 31722-917-01 D-0248-2018
Class III · Low risk Terminated

Ciclopirox Olamine Cream USP

Reason Discoloration: Product is supposed to be a white to off white homogenous cream and may have intermittent yellow discoloration.

G & W Laboratories, Inc. NDC 0713-0638-15 D-0250-2018
Class III · Low risk Terminated

Vecuronium bromide for Injection

Reason Failed impurities/ degradation specifications: Out-of-specification (OOS) result for USP related compound F at the 12 month stability test station.

Fresenius Kabi USA, LLC NDC 63323-781-10 D-0426-2018
Class III · Low risk Terminated

Simvastatin Tablets

Reason Presence of foreign substance: metallic razor blade was found in one bottle.

Hetero Labs, Ltd. - Unit III NDC 31722-513-10 D-0223-2018
Class III · Low risk Terminated

Clobetasol Propionate Cream USP

Reason Failed Content Uniformity Specifications

Taro Pharmaceuticals U.S.A., Inc. NDC 51672-1258-3 D-0249-2018
Class III · Low risk Terminated

Gabapentin Oral Solution

Reason CGMP Deviations: Inadvertent release of a drug product with unapproved active ingredient manufacturer.

Akorn Inc D-0211-2018
Class III · Low risk Terminated

Auryxia

Reason Presence of Foreign Substance: Reports have been received of damaged StripPax packets containing silica gel desiccant potentially allowing the silica gel granules to make contact with Auryxia tablets in the bottle.

Keryx Biopharmaceuticals, Inc. NDC 59922-631-01 D-0133-2018
Class III · Low risk Terminated

Enoxaparin Sodium

Reason 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

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

Bull Capsules

Reason Marketed without an Approved NDA/ANDA; product found to be tainted with sildenafil

BYL Solutions Inc. D-0414-2018