PlainRecalls
FDA Drug Moderate Class II Terminated

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

Reported: August 7, 2019 Initiated: July 22, 2019 #D-1576-2019

Product Description

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

Reason for Recall

Lack of Processing Controls

Details

Recalling Firm
Wise Pharmacy
Units Affected
32 vials
Distribution
CO, TX, WY
Location
Littleton, CO

Frequently Asked Questions

What product was recalled?
Papaverine/Phentolamine/Alprostadil 30 mg/2 mg/50 mcg/mL Injectable, 2.5 mL Vial, Rx only, Compounded by Wise Pharmacy, Littleton, CO 80123.. Recalled by Wise Pharmacy. Units affected: 32 vials.
Why was this product recalled?
Lack of Processing Controls
Which agency issued this recall?
This recall was issued by the FDA Drug on August 7, 2019. Severity: Moderate. Recall number: D-1576-2019.