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.

Papaverine/Phentolamine/Alprostadil/Atropine 30 mg/2 mg/50 mcg/0.15 mg/mL Injectable Recalled by Wise Pharmacy Due to Lack of Processing Controls

Date: July 22, 2019
Company: Wise Pharmacy
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 Wise Pharmacy directly.

Affected Products

Papaverine/Phentolamine/Alprostadil/Atropine 30 mg/2 mg/50 mcg/0.15 mg/mL Injectable, 2.5 mL Vial, Rx only, Compounded by Wise Pharmacy, Littleton, CO 80123.

Quantity: 14 vials

Why Was This Recalled?

Lack of Processing Controls

Where Was This Sold?

This product was distributed to 3 states: CO, TX, WY

Affected (3 states)Not affected

About Wise Pharmacy

Wise Pharmacy has 11 total recalls tracked by RecallDetector.

Related Recalls

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