FDAClass IIJune 17, 2015

Bimix (PHENT recall: Sterility Concern

Bimix (PHENT;PAP) (N), solution, (10/300) 1 - 30 mg/mL, injectable, 5ml vial, Rx only, compounded by Montana Compounding Pharmacy in Missoula, MT.

Why was Bimix (PHENT recalled?

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

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?

Lot 04102015:18@15, expiry date: 7/3/2015

Product
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
Quantity
1/5mL vial
Distribution
MT and ND
Recall date
June 17, 2015
Classification
Class II
Status
Terminated
Agency
FDA (drug)
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