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  1. FDA Recalls
  2. ›Drug Recalls

FDA Drug Recalls

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

Classification
AllClass IClass IIClass III
Status
AllOngoingCompletedTerminated
Date
All timePast 30 daysPast 12 months

Showing 7981–8000 of 17,773 recalls

Class IIITerminated

Oxytocin 30 Units added to NS 500 mL (oxytocin and 0.9% Sodium Chloride) Injectable Solution, Approximately 503 mL Sterile single use bag, Rx only, Avella of Houston, 9265 Kirby Dr., Houston, TX 77054, NDC 42852-706-50.

Advanced Pharma Inc.

Superpotent Drug: product may contain concentrations of oxytocin higher than what is represented on the label.

February 6, 2019 · DrugView details →
Class IIITerminated

Oxytocin 10 Units added to NS 1000 mL (oxytocin and 0.9% Sodium Chloride) Injectable Solution, Approximately 1001 mL Sterile single use bag, Rx only, Avella of Houston, 9265 Kirby Dr., Houston, TX 77054, NDC 42852-730-99.

Advanced Pharma Inc.

Superpotent Drug: product may contain concentrations of oxytocin higher than what is represented on the label.

February 6, 2019 · DrugView details →
Class IITerminated

Advanced Gel Hand Sanitizer (Ethyl alcohol 62%), packaged in a) 37 mL (1.25 fl oz) bottles (NDC 47593-488-49) and b) 540 mL (18 fl oz) bottles (NDC 47593-488-31) Ecolab, 370 Wabasha Street N, St. Paul, MN 55102.

Ecolab Inc

Chemical Contamination: low levels of various substituted benzene (aromatic) compounds identified in the product after complaints of malodor.

February 6, 2019 · DrugView details →
Class IITerminated

Fentanyl in 0.9% Sodium Chloride QS 0.5 mL, 5 mcg/0.5 mL with up to 0.1 mL of overfill Injectable Solution, Sterile single use syringe, Rx only, Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404, NDC 42852-210-72

Advanced Pharma Inc.

Labeling: Incorrect expiration date.

February 6, 2019 · DrugView details →
Class IIITerminated

Esomeprazole Magnesium Delayed-Release Capsules USP, 40mg*, a) 90-count bottle (NDC 43598-510-90) b) 1000 count bottle (NDC 43598-510-10), Rx only, Mfd By: Dr. Reddy's Laboratories Limited Bachupally - 500 090 INDIA.

Dr. Reddy's Laboratories, Inc.

Discoloration: Esomeprazole Magnesium DR Capsules (40mg) may contain brown pellets.

February 6, 2019 · DrugView details →
Class IITerminated

Quick-Care Foam Hand Sanitizer (Ethyl alcohol 62%), 45 mL (1.5 fl oz) bottles, Ecolab, 370 Wabasha Street N, St. Paul, MN 55102. NDC 47593-491-85

Ecolab Inc

Chemical Contamination: low levels of various substituted benzene (aromatic) compounds identified in the product after complaints of malodor.

February 6, 2019 · DrugView details →
Class IITerminated

Gel Hand Sanitizer (Ethyl Alcohol 70%), packaged in a) 37 mL (1.25 fl oz) bottles (NDC 47593-487-49), b) 118 mL (4 fl oz) bottles (NDC 47593-487-33), and c) 540 mL (18 fl oz) bottles (NDC47593-487-31) Ecolab, 370 Wabasha Street N, St. Paul, MN 55102.

Ecolab Inc

Chemical Contamination: low levels of various substituted benzene (aromatic) compounds identified in the product after complaints of malodor.

February 6, 2019 · DrugView details →
Class IITerminated

Moisturizing Lubricant Eye Drops, 0.25% Sodium Carboxymethylcellulose, 0.5 Fl OZ (15mL) Distributed by: Walgreen Co, 200 Wilmont Rd Deerfield IL 60015 NDC 00363-9651-01.

Akorn Inc

Failed Stability Specification: out of specification results for Sodium Perborate

February 4, 2019 · DrugView details →
Class IITerminated

0.9% Sodium Chloride Injection, USP 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-7983-09

ICU Medical Inc

CGMP Deviations

February 4, 2019 · DrugView details →
Class IITerminated

Dymista (azelastine hydrochloride and fluticasone propionate) Nasal Spray, 137 mcg/50 mcg per spray, 120 Metered Sprays, 23 g net fill weight bottle, Rx Only, Manufactured by: Cipla Ltd., Goa, India, M.L. No. 546; For: Meda Pharmaceuticals Inc., Somerset, New Jersey 08873-4120, NDC 0037-0245-23.

Mylan Pharmaceuticals Inc.

Defective Container: Potential for broken glass in the neck area of the glass bottles.

February 1, 2019 · DrugView details →
Class ITerminated

Levoleucovorin Injection, 250 mg/25 mL, (10 mg/mL), 25 mL Single-Use Vial, Rx only, Manufactured for: Mylan Institutional LLC, Rockford, IL 61103 U.S.A., Made in India. NDC: 67457-601-30

Mylan Institutional Inc

Presence of Particulate Matter: particulate matter identified as copper salts

February 1, 2019 · DrugView details →
Class IIITerminated

Moxifloxacin Ophthalmic Solution USP, 0.5%, 3 mL dropper bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202 Manufactured by: lupin Limited Pithampur (M.P.) 454 775 India. NDC 68180-422-01

Lupin Pharmaceuticals Inc.

Failed Impurities/Degradation Specifications: Out of specification test results in related substance at three-month long term stability study was obtained.

February 1, 2019 · DrugView details →
Class IITerminated

Divalproex Sodium Extended-release Tablets, USP 250 mg, 100-count bottle, Rx only, Mfd.By: Dr. Reddy's Laboratories Limited Bachupally - 500 090 India NDC 55111-533-01

Dr. Reddy's Laboratories, Inc.

Failed Dissolution Specifications: Out of specification results observed for high dissolution.

January 31, 2019 · DrugView details →
Class IIITerminated

Cardizem CD (diltiazem HCl) capsules, 120 mg, packaged in a) 30-count bottles (NDC 0187-0795-30); and b) 90-count bottles (NDC 0187-0795-42), Rx Only, Manufactured for: Valeant Pharmaceuticals North America LLC, Bridgewater, NJ 08807 USA; By: Valeant Pharmaceuticals International, Inc., Steinbach, MB R5G 1Z7, Canada.

Valeant Pharmaceuticals North America LLC

Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.

January 30, 2019 · DrugView details →
Class IIITerminated

Diltiazem HCl CD capsules, 360 mg, 90-count bottles, Rx Only, Manufactured for: Oceanside Pharmaceuticals, a division of Valeant Pharmaceuticals North America LLC, Bridgewater, NJ 08807 USA; By: Valeant Pharmaceuticals International, Inc., Steinbach, MB R5G 1Z7 Canada; NDC 68682-521-01.

Valeant Pharmaceuticals North America LLC

Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.

January 30, 2019 · DrugView details →
Class IIITerminated

Cardizem CD (diltiazem HCl) capsules, 300 mg, packaged in a) 30-count bottles (NDC 0187-0798-30); and b) 90-count bottles (NDC 0187-0798-42), Rx Only, Manufactured for: Valeant Pharmaceuticals North America LLC, Bridgewater, NJ 08807 USA; By: Valeant Pharmaceuticals International, Inc., Steinbach, MB R5G 1Z7, Canada.

Valeant Pharmaceuticals North America LLC

Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.

January 30, 2019 · DrugView details →
Class IIITerminated

Cardizem CD (diltiazem HCl) capsules, 180 mg, packaged in a) 30-count bottles (NDC 0187-0796-30); and b) 90-count bottles (NDC 0187-0796-42), Rx Only, Manufactured for: Valeant Pharmaceuticals North America LLC, Bridgewater, NJ 08807 USA; By: Valeant Pharmaceuticals International, Inc., Steinbach, MB R5G 1Z7, Canada.

Valeant Pharmaceuticals North America LLC

Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.

January 30, 2019 · DrugView details →
Class IIITerminated

Cardizem CD (diltiazem HCl) capsules, 240 mg, packaged in a) 30-count bottles (NDC 0187-0797-30); and b) 90-count bottles (NDC 0187-0797-42), Rx Only, Manufactured for: Valeant Pharmaceuticals North America LLC, Bridgewater, NJ 08807 USA; By: Valeant Pharmaceuticals International, Inc., Steinbach, MB R5G 1Z7, Canada.

Valeant Pharmaceuticals North America LLC

Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.

January 30, 2019 · DrugView details →
Class IITerminated

Ephedrine Sulfate, 50 mg/10 mL, 10 mL Single Use Syringe, Rx only, US Compounding Pharmacy 1270 Don's Lane Conway, AR 800-718-3588, Barcode: 62295308407

US Compounding Inc

Lack of assurance of sterility.

January 29, 2019 · DrugView details →
Class IIITerminated

Bimatoprost Ophthalmic Solution 0.03%, packaged in a) 5 mL (NDC 68180-429-02) and b) 7.5 mL (NDC 68180-429-03) bottles, Rx only, Manufactured by: Lupin Limited Pithampur (M.P.) 454 775, INDIA.

Lupin Pharmaceuticals Inc.

Failed Impurities/Degradation Specifications: OOS results observed in any other individual impurity and total impurities.

January 28, 2019 · DrugView details →
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