FDAFDA · Food and drugs·Recall number D-0343-2017
Bimix 30 mg/1 mg/mL Injectable, a) 5 mL and b) 10 mL vial, Compounded by Wells Pharmacy Network, LLC, Ocala, FL
Published January 11, 2017 · Recall initiated: September 21, 2016
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Lack of Assurance of Sterility
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- Wells Pharmacy Network LLC
- Distributor
- Nationwide
- Lot
- All lot codes of product prepared between 02/22/2016 and 09/14/2016, within expiry. a) Known lot code: 04012016@7, 04252016@17, 05262016@13, 06142016@39, 08052016@13 b) Known lot code: 05242016@11, 09072016@18
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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