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FDA Recalls
›Drug Recalls

FDA Drug Recalls

Recalls of prescription drugs, over-the-counter medications, and compounded pharmaceuticals.

Classification

All Class I Class II Class III

Status

All Ongoing Completed Terminated

Date

All time Past 30 days Past 12 months

Showing 241–260 of 1,000 recalls

Class IIITerminated

DELFLEX Peritoneal Dialysis Solution with 1.5% Dextrose, Low magnesium, Low Calcium, packaged in a) 3000 mL bags (NDC 49230-206-30) and b) 5000mL bags, 2 packs (NDC 49230-206-50), Rx only, Fresenius Medical Care NA, Waltham, MA 02451

Fresenius Medical Care Holdings, Inc.

Temperature Abuse: Product exposed to temperature outside specified limits.

April 28, 2021 · DrugView details →

Class IIITerminated

DELFLEX Peritoneal Dialysis Solution with 1.5% Dextrose, Low magnesium, Low Calcium and attached stay safe Exchange set, 2000 mL Fresenius Medical Care NA, Waltham, MA 02451, NDC 49230-206-92

Fresenius Medical Care Holdings, Inc.

Temperature Abuse: Product exposed to temperature outside specified limits.

April 28, 2021 · DrugView details →

Class IIITerminated

DELFLEX Peritoneal Dialysis Solution with 1.5% Dextrose, 5000 mL bags, 2-pack, Rx Only, Fresenius Medical Care NA, Waltham, MA 02451, NDC 49230-0188-50

Fresenius Medical Care Holdings, Inc.

Temperature Abuse: Product exposed to temperature outside specified limits.

April 28, 2021 · DrugView details →

Class IIITerminated

Hydrocodone Bitartrate and Homatropine Methlybromide tablets, USP, 5 mg/ 1.5 mg, 30-count bottle, Rx only, Mfd. By:KVK-Tech, Inc., Newtown, PA, 18940 NDC 10702-055-03

KVK-Tech, Inc.

Failed Impurities/Degradation Specifications

April 27, 2021 · DrugView details →

Class IIITerminated

Acyclovir Tablets, USP, 400 mg, 100 Tablets, Rx Only, Distributed by: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816, NDC 23155-227-01. Packaged in 150 cc white HDPE bottle

Heritage Pharmaceuticals Inc

Labeling: Incorrect or Missing Lot and/or Exp Date

April 21, 2021 · DrugView details →

Class IIITerminated

Evrysdi (risdiplam) for oral solution, 60 mg/80mL (0.75mg/mL), 80 mL total volume after constitution, Rx only, Distributed by: Genentech, Inc. NDC:50242-175-05

Genentech Inc

Defective Container: complaints received regarding some incorrect press-in-bottle-adapters (PIBA), the incorrect PIBAs have a female instead of male fit so they cannot be used in combination with co-packed syringes.

April 20, 2021 · DrugView details →

Class IIITerminated

Asenapine Sublingual Tablets, 5 mg, Rx Only, 60 Tablets, Sigmapharm Laboratories, LLC, Bensalem, PA, 19020 NDC 42794-016-10.

SigmaPharm Laboratories LLC

Incorrect Product Formulation; product was manufactured with the incorrect Art Cherry Flavor flavoring agent instead of Art Black Cherry Flavor flavoring agent

April 19, 2021 · DrugView details →

Class IIITerminated

Asenapine Sublingual Tablets, 10 mg, Rx only, 60 Tablets, Sigmapharm Laboratories, LLC, Bensalem, PA, 19020, NDC 42794-017-10

SigmaPharm Laboratories LLC

Incorrect Product Formulation; product was manufactured with the incorrect Art Cherry Flavor flavoring agent instead of Art Black Cherry Flavor flavoring agent

April 19, 2021 · DrugView details →

Class IIITerminated

Dry Eye Test, Fluorescein Sodium, Ophthalmic Strips USP (0.12mg Fluorescein Sodium), 100 Sterile Strips (50 Pouches of 2 Strips Each), Manufactured by: Nomax, Inc, St. Louis, MO 63123, NDC: 51801-008-15

Nomax Inc

Subpotent Drug

April 13, 2021 · DrugView details →

Class IIITerminated

Lidocaine Ointment USP, 5%, NET WT 35.44 g (1 1/4 Oz) tube, Rx Only, Teligent Pharma Inc., Buena, New Jersey, 08310, NDC 52565-008-14.

Teligent Pharma, Inc.

Failed Stability Specifications: product did not meet viscosity results.

March 29, 2021 · DrugView details →

Class IIITerminated

Metformin HCl Extended-Release Tablets, USP, 500 mg, Rx Only, 500-count bottle, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512; Manufactured by: Sun Pharmaceutical Industries Ltd., Halol-Baroda HIghway, Halol-389 350 Gujarat, India, NDC 62756-142-02.

SUN PHARMACEUTICAL INDUSTRIES INC

Failed Moisture Limits: Out of specification for water content

March 25, 2021 · DrugView details →

Class IIITerminated

Candesartan Cilexetil Tablets, USP, 4 mg, 30-count bottles, Rx only, Manufactured for: Macleods Pharma USA, Inc., Plainsboro, NJ 08536, Manufactured by: Macleods Pharmaceuticals Ltd., Daman (U.T.), India, NDC 33342-114-10

Macleods Pharma Usa Inc

Failed Impurities/Degradation Specifications

March 22, 2021 · DrugView details →

Class IIITerminated

Sp-4, 100 mL solution bottles, Rx only, Washington Homeopathic Products, Inc.260 J R Hawvermale Way Berkeley Springs West Virginia 25411

Washington Homeopathic Products, Inc.

An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.

March 18, 2021 · DrugView details →

Class IIITerminated

LCL-2-0191, 5 gallon carboys, Rx only, Manufactured for: LaCore Labs, LLC, by: Washington Homeopathic Products, Inc.260 J R Hawvermale Way Berkeley Springs West Virginia 25411

Washington Homeopathic Products, Inc.

An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.

March 18, 2021 · DrugView details →

Class IIITerminated

Macula Pellets Homeopathic Medicine, 1 Oz bottles, Rx only, Manufactured for: Natural Ophthalmics Inc. PO Box 1510 Dillon, CO 80435, NDC 58770-190-42

Washington Homeopathic Products, Inc.

An error occurred where the product was manufactured with Potassium Chloride instead of Potassium Phosphate.

March 18, 2021 · DrugView details →

Class IIITerminated

Tremfya (guselkumab) Injection, 100 mg/mL, one single-dose prefilled syringe per carton, Rx only, Manufactured by: Janssen Biotech, Inc., Horsham, PA 19044; NDC 57894-640-01.

Cardinal Health Inc.

Temperature Abuse

March 9, 2021 · DrugView details →

Class IIITerminated

Romidepsin Injecton, 27.5 mg/5.5 mL (5 mg/mL) Rx Only, 5.5 ml vial, Teva Pharmaceuticals USA, Inc. NDC 0703-4004-01

Teva Pharmaceuticals USA

Failed Impurity/Degradation Specifications: Out-of-specifications results observed for impurities during stability testing.

March 4, 2021 · DrugView details →

Class IIITerminated

Menopur 75 IU, (menotropins for injection), packaged as a) 5 single dose vials of Menotropins for injection, 5 single dose vials of 0.9% Sodium Chloride Injection, USP 2 mL, NDC 55566-7501-2; b) Professional Sample Kit: 3 single dose vials of Menotropins for injection, 3 single dose vials of 0.9% Sodium Chloride Injection, USP 2 mL, NDC 55566-7501-3; Rx Only, Manufactured for Ferring Pharmaceuticals Inc. Parsippany. NJ 07054. Diluent manufactured for Ferring Pharmaceuticals Inc.

Ferring Pharmaceuticals Inc

Failed pH specifications: Out of Specification pH results for 0.9% Sodium Chloride, USP

March 2, 2021 · DrugView details →

Class IIITerminated

Cequa (cyclosporine ophthalmic solution) 0.09%, 60 Single-Use Vials (6 pouches x 10 single-use vials (0.25 mL each)), Rx only, Manufactured for Sun Pharma Global FZE by: Laboratoire Unither, Coutances, France NDC 47335-506-96

SUN PHARMACEUTICAL INDUSTRIES INC

Subpotent

February 22, 2021 · DrugView details →

Class IIITerminated

Methylprednisolone Tablets USP, 4 MG, packaged in a 21-count blister pack, Rx only, Jubilant Cadista Pharmaceuticals, Inc., Salisbury, MD 21801, NDC 59746-001-03

Jubilant Cadista Pharmaceuticals, Inc.

Labeling: Illegible label: Customer complaint received of mis-alignment print of the printed dosing instructions on the blister card.

February 19, 2021 · DrugView details →

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