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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 12,941–12,960 of 17,974 drug recalls

Drug Recall Terminated Historical recordClass II

Nandrolone 200 mg/ml Injection, 10 mL and 20 mL vials, Rx, B & B Health Mart Pharmacy, Bellflower, CA

by Pacific Healthcare, Inc dba B&B Pharmacy

Reason
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility
Recall initiated
October 7, 2015
Reported by FDA
November 18, 2015
Distribution
CA and NJ

View recall →

Drug Recall Terminated Historical recordClass II

Stanozolol 200 mg/ml Injection, 20 mL vial, Rx, B & B Health Mart Pharmacy, Bellflower, CA

by Pacific Healthcare, Inc dba B&B Pharmacy

Reason
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility
Recall initiated
October 7, 2015
Reported by FDA
November 18, 2015
Distribution
CA and NJ

View recall →

Drug Recall Terminated Historical recordClass II

Doxycycline Hyclate Tablets, USP, 100 mg, 500-count bottle, Rx only, Distributed by: Truxton Inc. Bellmawr, NJ 08031, Manufactured for: Blu Caribe Dorado, PR 00646 USA, NDC 0463-6000-50 (top panel) NDC 24658-312-05 (side panel)

by C. O. Truxton

Reason
Labeling: Wrong Bar Code
Recall initiated
August 24, 2015
Reported by FDA
November 18, 2015
Distribution
Nationwide

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Drug Recall Terminated Historical recordClass II

Fenoglide (fenofibrate) tablets, 120 mg Tablets, 90 Ct Bottle, Rx Only. Distributed by: Santarus, Inc. San Diego, CA 92130. NDC: 68012-495-90.

by Valeant Pharmaceuticals North America LLC

Reason
Failed Dissolution Specifications: Failed 24 month dissolution testing.
Recall initiated
September 4, 2015
Reported by FDA
November 11, 2015
Distribution
U.S. Nationwide

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Drug Recall Terminated Historical recordClass III

RANITIDINE SYRUP (RANITIDINE ORAL SOLUTION, USP) 15 mg/mL (75 mg/5 mL), 473 mL (16 fl oz), Rx only. Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC: 0603-9418-58.

by Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals

Reason
Failed Stability Specifications: Out of Specification results obtained for preservative butylparaben.
Recall initiated
October 21, 2015
Reported by FDA
November 11, 2015
Distribution
U.S. Nationwide

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Drug Recall Terminated Historical recordClass II

Xanax (alprazolam) tablets, 0.25 mg, 100-count bottle, Rx only, Distributed by Pharmacia & Upjohn Co. Division of Pfizer Inc, NY, NY 10017, NDC 0009-0029-01

by Pfizer Inc.

Reason
Subpotent Drug
Recall initiated
September 24, 2015
Reported by FDA
November 4, 2015
Distribution
Nationwide

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Drug Recall Terminated Historical recordClass II

TRI-MIX 20MCG+0.5MG+15MG/ML, 10 mL vial, Rx only, Park Compounding Pharmacy 280 N. Westlake Blvd., Ste. 100 Westlake Village, CA 91362, (805) 497-8258

by Chen Shwezin, Inc. dba Park Compounding Pharmacy

Reason
Lack of Assurance of Sterility: all sterile compounded products within expiry
Recall initiated
October 6, 2015
Reported by FDA
November 4, 2015
Distribution
CA

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Drug Recall Terminated Historical recordClass II

CAFFEINE + SODIUM BENZOATE 500MG/ML, 35 mL vial, Rx only, Park Compounding Pharmacy 280 N. Westlake Blvd., Ste. 100 Westlake Village, CA 91362, (805) 497-8258

by Chen Shwezin, Inc. dba Park Compounding Pharmacy

Reason
Lack of Assurance of Sterility: all sterile compounded products within expiry
Recall initiated
October 6, 2015
Reported by FDA
November 4, 2015
Distribution
CA

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Drug Recall Terminated Historical recordClass II

TRI-MIX 10MCG+0.5MG+15MG/ML,5 mL vial, Rx only, Park Compounding Pharmacy 280 N. Westlake Blvd., Ste. 100 Westlake Village, CA 91362, (805) 497-8258

by Chen Shwezin, Inc. dba Park Compounding Pharmacy

Reason
Lack of Assurance of Sterility: all sterile compounded products within expiry
Recall initiated
October 6, 2015
Reported by FDA
November 4, 2015
Distribution
CA

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Drug Recall Terminated Historical recordClass II

METHYLCOBALAMIN 1000MCG/ML, 10mL vial, Rx only, Park Compounding Pharmacy 280 N. Westlake Blvd., Ste. 100 Westlake Village, CA 91362, (805) 497-8258

by Chen Shwezin, Inc. dba Park Compounding Pharmacy

Reason
Lack of Assurance of Sterility: all sterile compounded products within expiry
Recall initiated
October 6, 2015
Reported by FDA
November 4, 2015
Distribution
CA

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Drug Recall Terminated Historical recordClass II

PROSTAGLANDIN PGE-1 40MCG/ML, 10mL vial, Rx only, Park Compounding Pharmacy 280 N. Westlake Blvd., Ste. 100 Westlake Village, CA 91362, (805) 497-8258

by Chen Shwezin, Inc. dba Park Compounding Pharmacy

Reason
Lack of Assurance of Sterility: all sterile compounded products within expiry
Recall initiated
October 6, 2015
Reported by FDA
November 4, 2015
Distribution
CA

View recall →

Drug Recall Terminated Historical recordClass II

VITAMIN D3 OIL, Injectable Solution, 50,000 UNITS/ML, syringe sizes: 10 mL and 30 mL, Rx only,JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314

by JD & SN Inc., dba Moses Lake Professional Pharmacy

Reason
Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recall initiated
July 24, 2015
Reported by FDA
November 4, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

VITAMIN D3 OIL, Injectable Solution, 400,000 UNITS/ML, syringe size: 20 mL, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314

by JD & SN Inc., dba Moses Lake Professional Pharmacy

Reason
Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recall initiated
July 24, 2015
Reported by FDA
November 4, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

VITAMIN B-COMPLEX, Injectable Solution, Syringe size: 30 mL, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314

by JD & SN Inc., dba Moses Lake Professional Pharmacy

Reason
Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recall initiated
July 24, 2015
Reported by FDA
November 4, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

TRIMIX, injectable Solution, 40MG/2MG/40MCG/ML, syringe size: 10mL, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314

by JD & SN Inc., dba Moses Lake Professional Pharmacy

Reason
Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recall initiated
July 24, 2015
Reported by FDA
November 4, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

TRIMIX, injectable Solution, 30MG/2MG/20MCG, syringe size: 10mL, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314

by JD & SN Inc., dba Moses Lake Professional Pharmacy

Reason
Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recall initiated
July 24, 2015
Reported by FDA
November 4, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

TRIMIX, injectable Solution, 30MG/1MG/20MCG, 10mL syringe, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314

by JD & SN Inc., dba Moses Lake Professional Pharmacy

Reason
Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recall initiated
July 24, 2015
Reported by FDA
November 4, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

TRIMIX, injectable Solution, 30MG/1MG/10MCG, syringe sizes: 5 mL and 10mL, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314

by JD & SN Inc., dba Moses Lake Professional Pharmacy

Reason
Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recall initiated
July 24, 2015
Reported by FDA
November 4, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

TRIMIX, injectable Solution, 20MG/1MG/20MCG/ML, 10mL syringe, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314

by JD & SN Inc., dba Moses Lake Professional Pharmacy

Reason
Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recall initiated
July 24, 2015
Reported by FDA
November 4, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

TRIMIX, injectable Solution, 15MG/.5MG/5MCG/ML, 10mL syringe, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314

by JD & SN Inc., dba Moses Lake Professional Pharmacy

Reason
Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Recall initiated
July 24, 2015
Reported by FDA
November 4, 2015
Distribution
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.