Trimix Injectable 30 mg/3 mg/60 mcg/mL recall: Sterility Concern
Trimix Injectable 30 mg/3 mg/60 mcg/mL, a) 2 mL, b) 5 mL and c) 10 mL vials, Compounded by Wells Pharmacy, Ocala, FL
Why was Trimix Injectable 30 mg/3 mg/60 mcg/mL 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: 07192016@27 b) Knonw lot code: 06202016@162 c) Known lot code: 07262016@49.
- Product
- Trimix Injectable 30 mg/3 mg/60 mcg/mL, a) 2 mL, b) 5 mL and c) 10 mL vials, Compounded by Wells Pharmacy, Ocala, FL
- Recalling firm
- Wells Pharmacy Network LLC
- Quantity
- a) 2 vials,, b) 9 vials and 6 vials
- Distribution
- Nationwide
- Recall date
- January 11, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)