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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 3,921–3,940 of 17,937 drug recalls

Drug Recall Terminated Historical recordClass II

Losartan Potassium Tablets, USP, 50 mg, Rx Only, Manufactured by: Vivimed Life Sciences Private Limited, Plot No., 101, 102, 107 & 108, SIDCO Pharmaceutical Complex, Alathur, Kanchipuram - 603 110, Tamilnadu, India, Distributed by: Strides Pharma Inc., East Brunswick, NJ 08816. 90 film coated tablets NDC 64380-934-05 1000 film coated tablets NDC 64380-934-08

by Strides Pharma Inc.

Reason
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recall initiated
May 18, 2022
Reported by FDA
June 8, 2022
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Phenylephrine HCl Injection, USP, 0.4 mg/10 mL (40 mcg/mL), 10 mL Pre-Filled Syringe, 5 x 10 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-955-10

by Nephron Sterile Compounding Center LLC

Reason
Lack of Assurance of Sterility
Recall initiated
May 18, 2022
Reported by FDA
June 8, 2022
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Neostigmine Methylsulfate Injection, USP, 5 mg/5 mL (1 mg/mL), Preservative Free, 5 mL Pre-Filled Syringe, 5 x 5 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only Nephron 503B outsourcing facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-902-05

by Nephron Sterile Compounding Center LLC

Reason
Lack of Assurance of Sterility
Recall initiated
May 18, 2022
Reported by FDA
June 8, 2022
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Lidocaine HCl Injection, USP, 2%, 100 mg/5 mL (20 mg/mL), Preservative Free, 5 mL Pre-Filled Syringe, 5 x 5 mL Pre-FIlled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-949-05

by Nephron Sterile Compounding Center LLC

Reason
Lack of Assurance of Sterility
Recall initiated
May 18, 2022
Reported by FDA
June 8, 2022
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Ketamine Hydrochloride Injection, USP, 50 mg/5 mL (10 mg/mL), 5 mL Pre-Filled Syringe, 5 x 5 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-982-55

by Nephron Sterile Compounding Center LLC

Reason
Lack of Assurance of Sterility
Recall initiated
May 18, 2022
Reported by FDA
June 8, 2022
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Hydromorphone HCl Injection, USP, 6 mg/30 mL (0.2 mg/mL), 30 mL Pre-Filled Syringe, 5 x 30 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-529-30

by Nephron Sterile Compounding Center LLC

Reason
Lack of Assurance of Sterility
Recall initiated
May 18, 2022
Reported by FDA
June 8, 2022
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Glycopyrrolate Injection, USP, 0.6 mg/3 mL (0.2 mg/mL), Preservative Free, 3 mL Pre-Filled Syringe, 5 x 3 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-903-03

by Nephron Sterile Compounding Center LLC

Reason
Lack of Assurance of Sterility
Recall initiated
May 18, 2022
Reported by FDA
June 8, 2022
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Epinephrine Injection, USP, 1 mg/10 mL (100 mcg/mL), 10 mL Pre-Filled Syringe, 5 x 10 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-925-10

by Nephron Sterile Compounding Center LLC

Reason
Lack of Assurance of Sterility
Recall initiated
May 18, 2022
Reported by FDA
June 8, 2022
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Calcium Gluconate Injection, USP 10%, 0.465 mEq Ca++/mL, 1 g/10 mL (100 mg/mL), 10 mL Pre-Filled Syringe, 5 x 10 Pre-filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-950-10

by Nephron Sterile Compounding Center LLC

Reason
Lack of Assurance of Sterility
Recall initiated
May 18, 2022
Reported by FDA
June 8, 2022
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass I

Benzonatate capsules, 100mg, repackaged in 30-count bottles, Distributed by Calvin Scott & Co., Inc, Albuq., NM. 87123, NDC 67877-0573-05

by Calvin Scott & Company, Inc.

Reason
Labeling: Label Mix-up: Bottle labeled as Benzonatate 100 mg capsules contained Benzphetamine 50 mg tablets and a bottle labeled as Benzphetamine 50 mg tablets contained Benzonatate 100 mg capsules.
Recall initiated
January 15, 2021
Reported by FDA
June 1, 2022
Distribution
1 physician in Alpharetta, GA

View recall →

Drug Recall Terminated Historical recordClass III

Benzphetamine tablets, 50mg, CIII, repackaged in 30-count bottles, Distributed by Calvin Scott & Co., Inc, Albuq., NM. 87123, NDC 10702-0040-50

by Calvin Scott & Company, Inc.

Reason
Labeling: Label Mix-up: Bottle labeled as Benzonatate 100 mg capsules contained Benzphetamine 50 mg tablets and a bottle labeled as Benzphetamine 50 mg tablets contained Benzonatate 100 mg capsules.
Recall initiated
January 15, 2021
Reported by FDA
June 1, 2022
Distribution
1 physician in Alpharetta, GA

View recall →

Drug Recall Completed Historical recordClass II

Amino Blend Glutamine 30 mg/mL Ornithine HCL 50 mg/mL Arginine HCL 100 mg/mL Lysine HCL 50 mg/mL Citrulline 50 mg/mL, Multi-Dose 30 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835.NDC 73198-0129-30.

by Olympia Compounding Pharmacy dba Olympia Pharmacy

Reason
Lack of assurance of sterility.
Recall initiated
May 9, 2022
Reported by FDA
June 1, 2022
Distribution
Distributed Nationwide in th USA, Puerto Rico and US Virgin Islands

View recall →

Drug Recall Completed Historical recordClass II

QM-3 Papaverine 30 mg/mL Phentolamine 3 mg/mL Alprostadil 150 mcg/mL Atropine 0.2 mg/mL, Multi-Dose 10 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835. NDC 73198-0019-10.

by Olympia Compounding Pharmacy dba Olympia Pharmacy

Reason
Lack of assurance of sterility.
Recall initiated
May 9, 2022
Reported by FDA
June 1, 2022
Distribution
Distributed Nationwide in th USA, Puerto Rico and US Virgin Islands

View recall →

Drug Recall Completed Historical recordClass II

QM-2 Papaverine 30 mg/mL Phentolamine 3 mg/mL Alprostadil 60 mcg/mL Atropine 0.2 mg/mL Multi-Dose 10 mL Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835. NDC 73198-0018-10.

by Olympia Compounding Pharmacy dba Olympia Pharmacy

Reason
Lack of assurance of sterility.
Recall initiated
May 9, 2022
Reported by FDA
June 1, 2022
Distribution
Distributed Nationwide in th USA, Puerto Rico and US Virgin Islands

View recall →

Drug Recall Completed Historical recordClass II

Pyridoxine HCL 100 mg/mL, Multi-Dose 30 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835. NDC 73198-0066-30.

by Olympia Compounding Pharmacy dba Olympia Pharmacy

Reason
Lack of assurance of sterility.
Recall initiated
May 9, 2022
Reported by FDA
June 1, 2022
Distribution
Distributed Nationwide in th USA, Puerto Rico and US Virgin Islands

View recall →

Drug Recall Completed Historical recordClass II

Phenylephrine 1 mg/mL, Multi-Dose 5 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835. NDC 73198-0021-05.

by Olympia Compounding Pharmacy dba Olympia Pharmacy

Reason
Lack of assurance of sterility.
Recall initiated
May 9, 2022
Reported by FDA
June 1, 2022
Distribution
Distributed Nationwide in th USA, Puerto Rico and US Virgin Islands

View recall →

Drug Recall Completed Historical recordClass II

PGE-3 Alprostadil 150 mcg/mL, Multi-Dose 10 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835. NDC 73198-0030-10.

by Olympia Compounding Pharmacy dba Olympia Pharmacy

Reason
Lack of assurance of sterility.
Recall initiated
May 9, 2022
Reported by FDA
June 1, 2022
Distribution
Distributed Nationwide in th USA, Puerto Rico and US Virgin Islands

View recall →

Drug Recall Completed Historical recordClass II

Ondansetron Hydrochloride, 1 mg/mL, Multi-Dose 30 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835. NDC 73198-0127-30.

by Olympia Compounding Pharmacy dba Olympia Pharmacy

Reason
Lack of assurance of sterility.
Recall initiated
May 9, 2022
Reported by FDA
June 1, 2022
Distribution
Distributed Nationwide in th USA, Puerto Rico and US Virgin Islands

View recall →

Drug Recall Completed Historical recordClass II

Olympia Vita-Complex Thiamine HCL (B1) 100 mg/mL Niacinamide (B3) 100 mg/mL Riboflavin 5 P04 (B2) 2 mg/mL Dexpanthenol (B5) 2 mg/mL Pyridoxine HCL (B6) 2 mg/mL Multi-Dose 30 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835. NDC 73198-0063-30.

by Olympia Compounding Pharmacy dba Olympia Pharmacy

Reason
Lack of assurance of sterility.
Recall initiated
May 9, 2022
Reported by FDA
June 1, 2022
Distribution
Distributed Nationwide in th USA, Puerto Rico and US Virgin Islands

View recall →

Drug Recall Completed Historical recordClass II

Olympia Mineral Blend Magnesium Chloride 80 mg/mL Zinc Sulfate 1 mg/mL Manganese Sulfate 20 mcg/mL Copper Gluconate 0.2 mg/mL Sodium Selenite 18 mcg/mL, Multi-Dose 30 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835. NDC 73198-0061-30.

by Olympia Compounding Pharmacy dba Olympia Pharmacy

Reason
Lack of assurance of sterility.
Recall initiated
May 9, 2022
Reported by FDA
June 1, 2022
Distribution
Distributed Nationwide in th USA, Puerto Rico and US Virgin Islands

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.