Bimix 30 mg/1 mg/mL Injectable recall: Sterility Concern
Bimix 30 mg/1 mg/mL Injectable, a) 5 mL and b) 10 mL vial, Compounded by Wells Pharmacy Network, LLC, Ocala, FL
Why was Bimix 30 mg/1 mg/mL Injectable recalled?
Lack of Assurance of Sterility
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
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
- Product
- Bimix 30 mg/1 mg/mL Injectable, a) 5 mL and b) 10 mL vial, Compounded by Wells Pharmacy Network, LLC, Ocala, FL
- Recalling firm
- Wells Pharmacy Network LLC
- Quantity
- a) 80 vials, b) 23 vials
- Distribution
- Nationwide
- Recall date
- January 11, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)