FDA Drug Recalls

Recalls / Class II

Class IID-0909-2022

Product

T-105 Papaverine 30 mg/mL Phentolamine 1 mg/mL PGE 10 mcg/mL, Packaged as a) 2.5 mL Multi-Dose vial NDC 73198-0005-03; b) 5 mL Multi Dose vial, NDC 73198-0005-05, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835

Affected lot / code info
Lots: K41J09, K41I09 BUD: 11/9/2022; B24B22-22 BUD: 2/22/2023

Why it was recalled

Lack of assurance of sterility.

Recalling firm

Firm
Olympia Compounding Pharmacy dba Olympia Pharmacy
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
6700 Conroy Rd Ste 155, Orlando, Florida 32835-3515

Distribution

Quantity
3312 vials
Distribution pattern
Distributed Nationwide in th USA, Puerto Rico and US Virgin Islands

Timeline

Recall initiated
2022-05-09
FDA classified
2022-05-25
Posted by FDA
2022-06-01
Status
Completed

Source: openFDA Drug Enforcement endpoint. Recall record D-0909-2022. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.