PlainRecalls
FDA Drug Moderate Class II Terminated

Trimix (Alprostadil/Papaverine/Phentolamine) 10 mcg/20 mg/1 mg Injectable 5 mL vials, Rx only, Family Pharmacy of Statesville, Inc.

Reported: March 23, 2022 Initiated: August 6, 2020 #D-0661-2022

Product Description

Trimix (Alprostadil/Papaverine/Phentolamine) 10 mcg/20 mg/1 mg Injectable 5 mL vials, Rx only, Family Pharmacy of Statesville, Inc.

Reason for Recall

Lack of Assurance of Sterility

Details

Units Affected
5 vials
Distribution
NC only
Location
Statesville, NC

Frequently Asked Questions

What product was recalled?
Trimix (Alprostadil/Papaverine/Phentolamine) 10 mcg/20 mg/1 mg Injectable 5 mL vials, Rx only, Family Pharmacy of Statesville, Inc.. Recalled by Family Pharmacy of Statesville. Units affected: 5 vials.
Why was this product recalled?
Lack of Assurance of Sterility
Which agency issued this recall?
This recall was issued by the FDA Drug on March 23, 2022. Severity: Moderate. Recall number: D-0661-2022.