Olympia Compounding Pharmacy dba Olympia Pharmacy: Drug Recall
Recall #D-0720-2022 · 03/08/2022
Class III: Low Risk
Recall Details
- Recall Number
- D-0720-2022
- 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
- 493 vials.
Reason for Recall
Sub Potent
Product Description
Formula F9, Papaverine 0.9 mg/mL, Phentolamine 0.1 mg/mL, PGE 20 mcg/mL, Atropine 0.01 mg/mL, Multi-Dose 10 mL vial, Each ML contains: 0.5% Chlorobutanol NF, 0.005% Edetate Disodium Dihydrate USP, 2.74% Benzyl Alcohol NF, 5% Mannitol USP, 1% Sodium Metabisulfite NF, 1% Ethyl Alcohol USP, Sterile Water for Injection USP, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155, Orlando, FL 32835. NDC 73198-0004-10
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.