# FDA recall D-0804-2021

> **Prescription Labs Inc dba Greenpark** · Class II · drug recall initiated 2021-08-18.

## Product

Spironolactone Ophthalmic Solution 0.005 mg/mL, 15 mL bottles, Rx only, Greenpark Compounding Pharmacy

## Reason for recall

Lack of Assurance of Sterility

## Distribution

Nationwide within the United States

## Key facts

- **Recall number:** D-0804-2021
- **Recalling firm:** Prescription Labs Inc dba Greenpark
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2021-08-18
- **Report date:** 2021-09-22
- **Termination date:** 2023-08-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Houston, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0804-2021

## Citation

> AI Analytics. FDA recall D-0804-2021. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-0804-2021. Source: US FDA. Licensed CC0.

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