PlainRecalls
FDA Drug Moderate Class II Terminated

Bimix 30 mg/1 mg/mL Injectable, a) 5 mL and b) 10 mL vial, Compounded by Wells Pharmacy Network, LLC, Ocala, FL

Reported: January 11, 2017 Initiated: September 21, 2016 #D-0343-2017

Product Description

Bimix 30 mg/1 mg/mL Injectable, a) 5 mL and b) 10 mL vial, Compounded by Wells Pharmacy Network, LLC, Ocala, FL

Reason for Recall

Lack of Assurance of Sterility

Details

Units Affected
a) 80 vials, b) 23 vials
Distribution
Nationwide
Location
Ocala, FL

Frequently Asked Questions

What product was recalled?
Bimix 30 mg/1 mg/mL Injectable, a) 5 mL and b) 10 mL vial, Compounded by Wells Pharmacy Network, LLC, Ocala, FL. Recalled by Wells Pharmacy Network LLC. Units affected: a) 80 vials, b) 23 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 January 11, 2017. Severity: Moderate. Recall number: D-0343-2017.