FDA Drug Recalls

Recalls / Class II

Class IID-1126-2015

Product

Trimix (PGE1;PHENT;PAP) (N), injectable, (100/10/240) 10UG, 5 mL vial, Rx only, compounded by Montana Compounding Pharmacy, Missoula, MT

Affected lot / code info
Lot 03112015:17@5; Expiry date: 6/1/2015; Lot 04042015:61@2; Expiry date: 6/3/2015; Lot 05022015:11@2; Expiry date: 6/16/2015;

Why it was recalled

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

Recalling firm

Firm
Montana Compounding Pharmacy
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
111 N Higgins Ave, N/A, Missoula, Montana 59802-4437

Distribution

Quantity
25/5 mL. vials
Distribution pattern
MT and ND

Timeline

Recall initiated
2015-05-15
FDA classified
2015-06-09
Posted by FDA
2015-06-17
Terminated
2016-12-20
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1126-2015. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.