Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Spironolactone Ophthalmic Solution 0.005 mg/mL Recalled by Prescription Labs Inc dba Greenpark Due to Lack of Assurance of Sterility

Date: August 18, 2021
Company: Prescription Labs Inc dba Greenpark
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Prescription Labs Inc dba Greenpark directly.

Affected Products

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

Quantity: 350 bottles

Why Was This Recalled?

Lack of Assurance of Sterility

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Prescription Labs Inc dba Greenpark

Prescription Labs Inc dba Greenpark has 1 total recall tracked by RecallDetector.

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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report