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 →
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.