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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 9,741–9,760 of 17,974 drug recalls

Drug Recall Terminated Historical recordClass II

Testosterone/Finasteride/Anastrozole 120 mg/10 mg/4 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

Testosterone/Finasteride 60 mg/5 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

Testosterone/Estradiol 60 mg/6 mg pellet Amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800 Testosterone/Finasteride 60 mg/5 mg pellet Amber vial, twist top surrounded by a wrapper Testosterone/Finasteride 80mg/8mg pellet Amber vial, twist top surrounded by a wrapper Testosterone/Finasteride/Anastrozole 120 mg/10 mg/4 mg pellet Amber vial, twist top surrounded by a wrapper

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/Anastrozole 120 mg/8 mg pellets 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

Progesterone 50 mg (SD) pellets in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800 twist top surrounded by a wrapper,

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

Pregnenolone 100 mg (SD) 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

TM #1 (ALP 5.9/PAPAV 17.65/PHEN 0.59) Injectable solution, packaged in 3 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

Testosterone Cypionate 200mg/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

Nandrolone decanoate 200mg/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

Methionine 25mg/Inositol 50mg/Choline 50mg/ B12 1mg, packaged in a) 5 mL amber vial and b) 50mL 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

Methionine15mg/Inositol 50mg/Choline 100mg, packaged in a) 5mL and b) 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

Lipoic Acid 25mg/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

HCG 1000 units/mL, packaged in a) 2 mL and b) 6 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

Glutathione 200mg/mL, 10mL 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

Amantadine HCl Capsules, USP, 100 mg, 50 Capsules (5x10) Unite Dose, Rx Only, Manufactured for: AvKARE Inc. Pulaski, TN 38478 --- NDC 50268-069-15

by AVKARE Inc.

Reason
Failed Dissolution Specifications
Recall initiated
March 30, 2018
Reported by FDA
April 25, 2018
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass III

Vasopressin 50 Units added to 250 mL 0.9% Sodium Chloride Injection USP (0.2 units per mL), Rx only, PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sugar Land, TX 77478

by PharMEDium Services, LLC

Reason
cGMP deviations
Recall initiated
April 10, 2018
Reported by FDA
April 25, 2018
Distribution
MA, WA

View recall →

Drug Recall Terminated Historical recordClass III

Triamterene and Hydrochlorothiazide Tablets, USP, 75 mg/50 mg, 500-count bottles, Rx only, Manufactured by Sandoz, Inc., Princeton, NJ 08540, NDC 0781-5067-05.

by Sandoz Incorporated

Reason
Cross Contamination With Other Products: presence of unrelated ingredients (i.e. traces of Lisinopril, Mannitol, Iron, Calcium and Phosphorous).
Recall initiated
April 6, 2018
Reported by FDA
April 25, 2018
Distribution
Nationwide in the USA and Puerto Rico

View recall →

Drug Recall Terminated Historical recordClass II

WipeEssentials Wet Wipes (benzalkonium chloride 0.13%), 30-count pouches, Dist. by Diamond Wipes Int'l, Inc., Chino, CA 91710, UPC 7 66670 03988 6.

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

Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr) Contains: 30 Patches Rx Only NDC 68968-5552-3 Manufactured for Noven Therapeutics, LLC., Miami, FL 33186 by Noven Pharmaceuticals, Inc. Miami, FL 33186 1-877-567-7857

by Noven Pharmaceuticals, Inc.

Reason
Defective Delivery System: Out of specification for adhesive transfer.
Recall initiated
April 9, 2018
Reported by FDA
April 25, 2018
Distribution
Nationwide.

View recall →

Drug Recall Terminated Historical recordClass III

Decitabine for Injection, 50mg per vial, Rx only, Manufactured by: Cipla Ltd., Verna Goa, India, Manufactured for: Cipla USA, Inc., 1560 Sawgrass Corporate Parkway, Suite 130, Sunrise, FL 33323, NDC 69097-285-37

by InvaGen Pharmaceuticals, Inc.

Reason
Failed impurities/degradation specifications: Failure to water content and impurity
Recall initiated
March 5, 2018
Reported by FDA
April 18, 2018
Distribution
U.S.A. nationwide

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.