Drug Recall
Ongoing
Historical recordClass II
ITPP 50 mg/ml DMG 100 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
by Lowlite Investments, Inc. D/B/A Olympia Pharmacy
- Reason
- Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
- Recall initiated
- May 29, 2013
- Reported by FDA
- July 17, 2013
- Distribution
- Nationwide and PR
View recall →
Drug Recall
Ongoing
Historical recordClass II
Iodine 20 mg Injection, compounded by Olympia Pharmacy, Orlando, FL
by Lowlite Investments, Inc. D/B/A Olympia Pharmacy
- Reason
- Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
- Recall initiated
- May 29, 2013
- Reported by FDA
- July 17, 2013
- Distribution
- Nationwide and PR
View recall →
Drug Recall
Ongoing
Historical recordClass II
Idoxuridine 0.1% Injection, compounded by Olympia Pharmacy, Orlando, FL
by Lowlite Investments, Inc. D/B/A Olympia Pharmacy
- Reason
- Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
- Recall initiated
- May 29, 2013
- Reported by FDA
- July 17, 2013
- Distribution
- Nationwide and PR
View recall →
Drug Recall
Ongoing
Historical recordClass II
Hippiron 20 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
by Lowlite Investments, Inc. D/B/A Olympia Pharmacy
- Reason
- Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
- Recall initiated
- May 29, 2013
- Reported by FDA
- July 17, 2013
- Distribution
- Nationwide and PR
View recall →
Drug Recall
Ongoing
Historical recordClass II
HCG 125iu/0.25ml (550iu/ml), 3500iu and 10,000iu, compounded by Olympia Pharmacy, Orlando, FL
by Lowlite Investments, Inc. D/B/A Olympia Pharmacy
- Reason
- Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
- Recall initiated
- May 29, 2013
- Reported by FDA
- July 17, 2013
- Distribution
- Nationwide and PR
View recall →
Drug Recall
Ongoing
Historical recordClass II
HACC 270.1 Injection, compounded by Olympia Pharmacy, Orlando, FL
by Lowlite Investments, Inc. D/B/A Olympia Pharmacy
- Reason
- Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
- Recall initiated
- May 29, 2013
- Reported by FDA
- July 17, 2013
- Distribution
- Nationwide and PR
View recall →
Drug Recall
Ongoing
Historical recordClass II
Guanabenz 20 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
by Lowlite Investments, Inc. D/B/A Olympia Pharmacy
- Reason
- Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
- Recall initiated
- May 29, 2013
- Reported by FDA
- July 17, 2013
- Distribution
- Nationwide and PR
View recall →
Drug Recall
Ongoing
Historical recordClass II
Guanabenz 8 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
by Lowlite Investments, Inc. D/B/A Olympia Pharmacy
- Reason
- Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
- Recall initiated
- May 29, 2013
- Reported by FDA
- July 17, 2013
- Distribution
- Nationwide and PR
View recall →
Drug Recall
Ongoing
Historical recordClass II
Glutathione 200 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
by Lowlite Investments, Inc. D/B/A Olympia Pharmacy
- Reason
- Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
- Recall initiated
- May 29, 2013
- Reported by FDA
- July 17, 2013
- Distribution
- Nationwide and PR
View recall →
Drug Recall
Ongoing
Historical recordClass II
Gentamicin Sulfate 80 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
by Lowlite Investments, Inc. D/B/A Olympia Pharmacy
- Reason
- Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
- Recall initiated
- May 29, 2013
- Reported by FDA
- July 17, 2013
- Distribution
- Nationwide and PR
View recall →
Drug Recall
Ongoing
Historical recordClass II
Gentamicin 80 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
by Lowlite Investments, Inc. D/B/A Olympia Pharmacy
- Reason
- Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
- Recall initiated
- May 29, 2013
- Reported by FDA
- July 17, 2013
- Distribution
- Nationwide and PR
View recall →
Drug Recall
Ongoing
Historical recordClass II
Gentamicin 300 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
by Lowlite Investments, Inc. D/B/A Olympia Pharmacy
- Reason
- Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
- Recall initiated
- May 29, 2013
- Reported by FDA
- July 17, 2013
- Distribution
- Nationwide and PR
View recall →
Drug Recall
Ongoing
Historical recordClass II
Gentamicin 0.3% Injection, compounded by Olympia Pharmacy, Orlando, FL
by Lowlite Investments, Inc. D/B/A Olympia Pharmacy
- Reason
- Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
- Recall initiated
- May 29, 2013
- Reported by FDA
- July 17, 2013
- Distribution
- Nationwide and PR
View recall →
Drug Recall
Ongoing
Historical recordClass II
Gaba 50 mg/Mag Sulfate 50 mg/Taurine/Theanine 50 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
by Lowlite Investments, Inc. D/B/A Olympia Pharmacy
- Reason
- Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
- Recall initiated
- May 29, 2013
- Reported by FDA
- July 17, 2013
- Distribution
- Nationwide and PR
View recall →
Drug Recall
Ongoing
Historical recordClass II
Furosemide 50 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
by Lowlite Investments, Inc. D/B/A Olympia Pharmacy
- Reason
- Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
- Recall initiated
- May 29, 2013
- Reported by FDA
- July 17, 2013
- Distribution
- Nationwide and PR
View recall →
Drug Recall
Ongoing
Historical recordClass II
Fluphenazine 25 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
by Lowlite Investments, Inc. D/B/A Olympia Pharmacy
- Reason
- Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
- Recall initiated
- May 29, 2013
- Reported by FDA
- July 17, 2013
- Distribution
- Nationwide and PR
View recall →
Drug Recall
Ongoing
Historical recordClass II
Estradiol Cypionate 10 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
by Lowlite Investments, Inc. D/B/A Olympia Pharmacy
- Reason
- Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
- Recall initiated
- May 29, 2013
- Reported by FDA
- July 17, 2013
- Distribution
- Nationwide and PR
View recall →
Drug Recall
Ongoing
Historical recordClass II
Enrofloxacin 20 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
by Lowlite Investments, Inc. D/B/A Olympia Pharmacy
- Reason
- Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
- Recall initiated
- May 29, 2013
- Reported by FDA
- July 17, 2013
- Distribution
- Nationwide and PR
View recall →
Drug Recall
Ongoing
Historical recordClass II
Doxapram 20 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
by Lowlite Investments, Inc. D/B/A Olympia Pharmacy
- Reason
- Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
- Recall initiated
- May 29, 2013
- Reported by FDA
- July 17, 2013
- Distribution
- Nationwide and PR
View recall →
Drug Recall
Ongoing
Historical recordClass II
Disodium EDTA Injection, compounded by Olympia Pharmacy, Orlando, FL
by Lowlite Investments, Inc. D/B/A Olympia Pharmacy
- Reason
- Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
- Recall initiated
- May 29, 2013
- Reported by FDA
- July 17, 2013
- Distribution
- Nationwide and PR
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.