# FDA recall D-0720-2022

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

## Product

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

## Reason for recall

Sub Potent

## Distribution

Nationwide in the USA including Puerto Rico.

## Key facts

- **Recall number:** D-0720-2022
- **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-0720-2022

## Citation

> AI Analytics. FDA recall D-0720-2022. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0720-2022. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*