Olympia Compounding Pharmacy dba Olympia Pharmacy: Drug Recall
Recall #D-0722-2022 · 03/08/2022
Class III: Low Risk
Recall Details
- Recall Number
- D-0722-2022
- Classification
- Class III
- Product Type
- Drug
- Recalling Firm
- Olympia Compounding Pharmacy dba Olympia Pharmacy
- Status
- Terminated
- Date Initiated
- 03/08/2022
- Location
- Orlando, FL, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1032 vials
Reason for Recall
Sub Potent
Product Description
SB-4, Papaverine 30mg/mL, Phentolamine 3mg/mL, Alprostadil 40mcg/mL, packaged in a) 5 mL Multi-dose vial NDC 73198-0023-05; b) 10 mL Multi-dose vial NDC 73198-0023-10, Each ML contains: 0.5% Chlorobutanol NF, 0.0005% Edetate Disodium Dihydrate USP, 1.84% Benzyl Alcohol NF, 5% Mannitol USP, 1% Sodium Metabisulfite NF, 2% Ethyl Alcohol USP, Sterile Water for Injection USP, Rx Only, Olympia Pharmaceuticals, Conroy Rd., Ste. 155, Orlando, FL 32835
Distribution Pattern
Nationwide in the USA including Puerto Rico.
Other Recalls by Olympia Compounding Pharmacy dba Olympia Pharmacy
- Class II: Risk 05/09/2022
- Class II: Risk 05/09/2022
- Class II: Risk 05/09/2022
- Class II: Risk 05/09/2022
- Class II: Risk 05/09/2022
View all recalls by Olympia Compounding Pharmacy dba Olympia Pharmacy →
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.