Bimix
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of Assurance of Sterility; objectionable conditions observed during a FDA inspection
What was recalled
Bimix (PHENT;PAP) (N), solution, (10/300) 1 - 30 mg/mL, injectable, 5ml vial, Rx only, compounded by Montana Compounding Pharmacy in Missoula, MT.
- Recalling firm
- Montana Compounding Pharmacy
- Origin
- MT, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-1120-2015
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
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