PlainRecalls
FDA Drug Moderate Class II Terminated

Trimix (A;PH,PA) (N), injectable, 160 UG-1.2 mg-9.6/ mg/mL, 2 mL vial, Rx only, compounded by Montana Compounding Pharmacy, Missoula, MT.

Reported: June 17, 2015 Initiated: May 15, 2015 #D-1125-2015

Product Description

Trimix (A;PH,PA) (N), injectable, 160 UG-1.2 mg-9.6/ mg/mL, 2 mL vial, Rx only, compounded by Montana Compounding Pharmacy, Missoula, MT.

Reason for Recall

Lack of Assurance of Sterility; objectionable conditions observed during a FDA inspection

Details

Units Affected
32/2 mL vials
Distribution
MT and ND
Location
Missoula, MT

Frequently Asked Questions

What product was recalled?
Trimix (A;PH,PA) (N), injectable, 160 UG-1.2 mg-9.6/ mg/mL, 2 mL vial, Rx only, compounded by Montana Compounding Pharmacy, Missoula, MT.. Recalled by Montana Compounding Pharmacy. Units affected: 32/2 mL vials.
Why was this product recalled?
Lack of Assurance of Sterility; objectionable conditions observed during a FDA inspection
Which agency issued this recall?
This recall was issued by the FDA Drug on June 17, 2015. Severity: Moderate. Recall number: D-1125-2015.