Drug Recall
Ongoing
Historical recordClass II
Vitamin B12 Cyanocobalamin 5000 mcg 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
Vitamin B12 (3000 mcg/ml & 5000 mcg/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
Vitamin A/D3/E Olive Oil 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
Vitamin 15 (HEMO15) 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
Tripelennamine 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
Trimix, 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
Testosterone Cypionate (100 mg/ml & 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
Tacrolimus (0.02% and 0.03%) drops, 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
Stanozolol (50 mg/ml and 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
Sodium Tetradecyl Sulfate (0.125%, 1%, 2.5%, 3%, and 4%) 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
Sodium Salicylate 40% 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
Sodium Iodide 20% 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
Sermorelin/GHRP 3 mg/3 mg vial, 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
Quadmix, 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
Progesterone EO 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
Progesterone 100 mg/ml in Olive Oil 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
Praziquantel 56.8mg/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
Potassium Phosphate 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
Phenylephrine 1 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
Phenylbutazone 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 →
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.