Drug Recall
Ongoing
Historical recordClass II
Diphenhydramine 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
Diclazuril 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
Dextrose 50% Solution, 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
Dexpanthenol 250 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
Dexamethasone Sodium Phosphate 6 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
Detomidine w/Xylazine 100 mg/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
Detomidine 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
Deslorelin 15 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
Cre-O-Pan 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
Clenbuterol 0.03mg/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
Chlorpromazine HCL 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
Cal-Phos 1000 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
Calcium Gluconate 23%, 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
Caco/Copper 6. 2 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
BNP/Dexamethasone Eye Ointment, 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
Bi mix, 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
Betamethasone Phosphate/Acetate 6 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
Betamethasone Sodium Phosphate 12 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
Beta Alanine 100 mg/ml / l-carnosine 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
Atropine Sulfate 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 →
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.