Recall Register

Drug recall: Alprostadil (PFE1), Solution, 10 mcg/mL, injectable, 5 mL vial, Rx only, compounded by Montana Compounding Pharmacy…

Class II FDA enforcement event 71275. Recall start date: . Status in the FDA record: Terminated. Termination date: .

Reason for recall, in the words of FDA

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

Class II, in the words of FDA

a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote

Montana Compounding Pharmacy started this drug recall on 15 May 2015. The firm address in the FDA record is in Missoula, MT. FDA put the recall in Class II. FDA event 71275 has 12 product records. The first FDA enforcement report date is 17 Jun 2015. The record gives the status Terminated, with the termination date 20 Dec 2016.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

MT and ND

Recalling firm

Montana Compounding Pharmacy, Missoula, MT.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

12 product records in the event.

FDA event 71275: product records
Recall numberProductQuantityClassStatusReport date
D-1117-2015Alprostadil (PFE1), Solution, 10 mcg/mL, injectable, 5 mL vial, Rx only, compounded by Montana Compounding Pharmacy, Missoula, MT1/5mL vialClass IITerminated17 Jun 2015
D-1118-2015Alprostadil (PFE1), solution, 20 mcg/mL, injectable, 5 mL vial, Rx only, compounded by Montana Compounding Pharmacy, Missoula, MT1/5 mL vialClass IITerminated17 Jun 2015
D-1119-2015Avastin, solution, 1.25 mg/0.05mL, Injectable, Syringe, Rx only, compounded by Montana Compounding Pharmacy, Missoula, MT259/0.05 mL SyringesClass IITerminated17 Jun 2015
D-1120-2015Bimix (PHENT;PAP) (N), solution, (10/300) 1 - 30 mg/mL, injectable, 5ml vial, Rx only, compounded by Montana Compounding Pharmacy in Missoula, MT.1/5mL vialClass IITerminated17 Jun 2015
D-1121-2015Glutathione INHALATION (PF), solution, 100mg/mL, 4 mL vial, Rx only, dispensed by Montana Compounding Pharmacy, Missoula, MT.20/4 mL vialsClass IITerminated17 Jun 2015
D-1122-2015Glutathione INHALATION (PF), NASAL solution, 100 mg/mL, 3 mL vial, Rx only, dispensed by Montana Compounding Pharmacy, Missoula, MT10/3 mL vialsClass IITerminated17 Jun 2015
D-1123-2015Hyaluronidase (RM ONLY), Injectable Solution, 150 U/mL, 10ML vial, Rx only, compounded by Montana Compounding Pharmacy, Missoula, MT20/1 mL vialsClass IITerminated17 Jun 2015
D-1124-2015Trimix (A;PH,PA) (N), injectable, 80 UG-0.6 mg-4.8 mg/mL, 1 mL vial, Rx only, compounded by Montana Compounding Pharmacy, Missoula, MT1/1 mL. vialClass IITerminated17 Jun 2015
D-1125-2015Trimix (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.32/2 mL vialsClass IITerminated17 Jun 2015
D-1126-2015Trimix (PGE1;PHENT;PAP) (N), injectable, (100/10/240) 10UG, 5 mL vial, Rx only, compounded by Montana Compounding Pharmacy, Missoula, MT25/5 mL. vialsClass IITerminated17 Jun 2015
D-1127-2015Trimix (PGE1;PHENT;PAP) (N), injectable, (100/10/297) 10UG, 5 mL vial, Rx only, compounded by Montana Compounding Pharmacy, Missoula, MT2/5 mL vialsClass IITerminated17 Jun 2015
D-1128-2015Alprostadil (PFE1), solution, 30 mcg/mL, injectable, 5 mL vial, Rx only, compounded by Montana Compounding Pharmacy, Missoula, MT1/5 mL vialClass IITerminated17 Jun 2015

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class II: The middle of the three FDA recall classes.

The event in context

Drug events that started in 2015
292
Share of these events in Class II
52%
Product records in this event
12
Events of the firm on the register
1

Official channels

Cite this page

Recall Register. FDA enforcement event 71275. https://recallregister.com/fda/ii/71275/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA drug enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: MT and ND
What quantity of product is in FDA event 71275?
The event has 12 product records. The first record gives this quantity: 1/5mL vial
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many drug recalls of 2015 have the same class?
52% of the 292 drug events that started in 2015 are in Class II.