# FDA recall D-0721-2022

> **Olympia Compounding Pharmacy dba Olympia Pharmacy** · Class III · drug recall initiated 2022-03-08.

## Product

T-105, Papaverine 30 mg/mL Phentolamine 1 mg/mL PGE 10 mcg/mL packaged as a) 5 mL Multi-dose NDC 73198-0005-05; b) 10 mL Multi-dose NDC 73198-0005-10; 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, 0.5% Ethyl Alcohol USP, Sterile Water for Injection USP, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155, Orlando, FL 32835.

## Reason for recall

Super Potent

## Distribution

Nationwide in the USA including Puerto Rico.

## Key facts

- **Recall number:** D-0721-2022
- **Recalling firm:** Olympia Compounding Pharmacy dba Olympia Pharmacy
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2022-03-08
- **Report date:** 2022-03-30
- **Termination date:** 2023-10-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Orlando, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0721-2022

## Citation

> AI Analytics. FDA recall D-0721-2022. Retrieved 2026-06-05 from https://api.ai-analytics.org/recall/D-0721-2022. Source: US FDA. Licensed CC0.

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