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FDA Drug Recalls

Every FDA drug enforcement recall Public Health Trace has on record, republished from openFDA's official drug enforcement database. See Health Alerts for current, active recalls alongside outbreaks and advisories.

Drug recall information is sourced from the FDA's structured openFDA Enforcement Reports. Newly announced recalls may appear on FDA.gov before they become available in the structured dataset. See Methodology for how Public Health Trace imports and refreshes this data.

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Showing 9,701–9,720 of 17,974 drug recalls

Drug Recall Terminated Historical recordClass II

Estradiol 40 mg (SD) pellets in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.

by Partell Specialty Pharmacy

Reason
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Recall initiated
March 22, 2018
Reported by FDA
April 25, 2018
Distribution
NV only

View recall →

Drug Recall Terminated Historical recordClass II

Estradiol 25 mg (SD) pellets in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.

by Partell Specialty Pharmacy

Reason
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Recall initiated
March 22, 2018
Reported by FDA
April 25, 2018
Distribution
NV only

View recall →

Drug Recall Terminated Historical recordClass II

Estradiol 20 mg (SD) pellets in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.

by Partell Specialty Pharmacy

Reason
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Recall initiated
March 22, 2018
Reported by FDA
April 25, 2018
Distribution
NV only

View recall →

Drug Recall Terminated Historical recordClass II

Testosterone 25 mg pellet packaged in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800

by Partell Specialty Pharmacy

Reason
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Recall initiated
March 22, 2018
Reported by FDA
April 25, 2018
Distribution
NV only

View recall →

Drug Recall Terminated Historical recordClass II

Testosterone 100 mg pellet packaged in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800

by Partell Specialty Pharmacy

Reason
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Recall initiated
March 22, 2018
Reported by FDA
April 25, 2018
Distribution
NV only

View recall →

Drug Recall Terminated Historical recordClass II

Testosterone 200 mg pellet packaged in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3

by Partell Specialty Pharmacy

Reason
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Recall initiated
March 22, 2018
Reported by FDA
April 25, 2018
Distribution
NV only

View recall →

Drug Recall Terminated Historical recordClass II

MVI-7 (B1-100mg/B3-100mg, B5-252 mg, B6-102mg, Vit C-2500 mg, B12-10mg, Mag-1000 mg)/ vial liquid injectable, 50 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800

by Partell Specialty Pharmacy

Reason
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Recall initiated
March 22, 2018
Reported by FDA
April 25, 2018
Distribution
NV only

View recall →

Drug Recall Terminated Historical recordClass II

Naltrexone 200 mg pellet, amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800

by Partell Specialty Pharmacy

Reason
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Recall initiated
March 22, 2018
Reported by FDA
April 25, 2018
Distribution
NV only

View recall →

Drug Recall Terminated Historical recordClass II

Methionine 25mg/Inositol 50mg/Choline 50mg/ B12 1mg, 50 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800

by Partell Specialty Pharmacy

Reason
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Recall initiated
March 22, 2018
Reported by FDA
April 25, 2018
Distribution
NV only

View recall →

Drug Recall Terminated Historical recordClass II

Vitamin D 50,000 unit/ml, 5 mL amber vial, Injectable Liquid, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. # 101, Las Vegas, NV 89119 (702) 791-3800

by Partell Specialty Pharmacy

Reason
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Recall initiated
March 22, 2018
Reported by FDA
April 25, 2018
Distribution
NV only

View recall →

Drug Recall Terminated Historical recordClass II

CoEnzymeQ10 25mg/mL, 5mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.

by Partell Specialty Pharmacy

Reason
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Recall initiated
March 22, 2018
Reported by FDA
April 25, 2018
Distribution
NV only

View recall →

Drug Recall Terminated Historical recordClass II

Biotin Suspension 10mg/mL, 5 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800

by Partell Specialty Pharmacy

Reason
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Recall initiated
March 22, 2018
Reported by FDA
April 25, 2018
Distribution
NV only

View recall →

Drug Recall Terminated Historical recordClass II

B-complex (B1-200mg, B2-4mg, B3-200mg,B5-4mg,B6-4mg) /mL, 5 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800

by Partell Specialty Pharmacy

Reason
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Recall initiated
March 22, 2018
Reported by FDA
April 25, 2018
Distribution
NV only

View recall →

Drug Recall Terminated Historical recordClass II

Ascorbic Acid (Tapioca) 500 mg/mL, 50 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800

by Partell Specialty Pharmacy

Reason
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Recall initiated
March 22, 2018
Reported by FDA
April 25, 2018
Distribution
NV only

View recall →

Drug Recall Terminated Historical recordClass II

ACURE, clarifying acne, glycolic + zinc (salicyclic acid 0.5%) towelettes, 30-count pouch, Distributed by Better Planet Brands, Fort Lauderdale, FL 33316, UPC 8 54049 00358 0.

by Diamond Wipes International, Inc.

Reason
CGMP Deviations: finished products were manufactured with poor quality water.
Recall initiated
April 2, 2018
Reported by FDA
April 25, 2018
Distribution
Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

PASTA DE LASSAR ANDROMACO Skin Protection, 25% zinc oxide Topical cream, 60 gram tube, UPC #851357003004, NDC #75940-111-60

by Marcas Usa Llc

Reason
Microbial Contamination of Non-Sterile Products
Recall initiated
March 30, 2018
Reported by FDA
April 25, 2018
Distribution
TX

View recall →

Drug Recall Terminated Historical recordClass II

Fluconazole Injection, USP, Iso-Osmotic Sodium Chloride Diluent, 200 mg in 100 mL (2 mg/mL), package in 100 mL bags, Rx only, Manufactured for: Claris Lifesciences Inc., North Brunswick, NJ 08902, By: Claris Injectables Limited, Sarkhei-Bavla Road, Chacharwadi-Vasna, Ahmedabad, India 382213, NDC 36000-002-10

by Renaissance Lakewood, LLC

Reason
Labeling: Label mix-up - A complaint was received of one bag of Fluconazole Injection, Iso-Osmotic Sodium Chloride Diluent, USP, 2mg/mL, 50 mL found within the package of 100 mL bags.
Recall initiated
February 21, 2018
Reported by FDA
April 25, 2018
Distribution
Product was distributed throughout the United States.

View recall →

Drug Recall Terminated Historical recordClass II

Lupin Cefdinir powder for Oral Suspension USP, 250 mg/5 mL in (a) 60 mL packs ( NDC 68180-723-20) and (b) 100 mL packs ( 68180-723-10), Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202

by Lupin Pharmaceuticals Inc.

Reason
Superpotent Drug
Recall initiated
March 27, 2018
Reported by FDA
April 25, 2018
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass III

Cystaran (cysteamine ophthalmic solution) 0.44%, 15 mL bottle, Rx only, Manufactured by Hi-Tech Pharmacal Co. Inc. Amityville, NY 11701 for Leadiant Biosciences, Inc. Gaithersburg, MD 20878, NDC 54482-020-01

by LEADIANT BIOSCIENCES, INC

Reason
Subpotent drug: Out of specification for an active ingredient cysteamine hydrochloride.
Recall initiated
April 9, 2018
Reported by FDA
April 25, 2018
Distribution
Walgreens Specialty Pharmacy Pittsburg, PA Italy and Germany

View recall →

Drug Recall Terminated Historical recordClass II

Testosterone/Finasteride 80 mg/8 mg pellet, amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.

by Partell Specialty Pharmacy

Reason
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Recall initiated
March 22, 2018
Reported by FDA
April 25, 2018
Distribution
NV only

View recall →

Data last updated:

This information is republished from FDA's Recall Enterprise System through openFDA. Public Health Trace does not verify or supplement it, is not affiliated with the FDA, and does not provide medical advice -- always follow the guidance of your pharmacist, physician, or the recalling company for any medication you take. Read the full medical disclaimer.