RecallRadar

FDA Drug recall D-1119-2015

Avastin, solution, 1.25 mg/0.05mL, Injectable, Syringe, Rx only, compounded by Montana Compounding Pharmacy, Missoula, MT

On 2015-06-17 the FDA classified a Class II recall of Avastin, solution, 1.25 mg/0.05mL, Injectable, Syringe, Rx only, compounded by Montana Compounding Pharmacy, Missoula, MT by Montana Compounding Pharmacy, citing lack of Assurance of Sterility; objectionable conditions observed during a FDA inspection.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1119-2015
ClassificationClass II
Statusterminated
Initiated2015-05-15
Published2015-06-17
Last updated2026-09-13 11:51 UTC
CompanyMontana Compounding Pharmacy
DistributionMT, ND

Product

Avastin, solution, 1.25 mg/0.05mL, Injectable, Syringe, Rx only, compounded by Montana Compounding Pharmacy, Missoula, MT

Reason

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

Identifiers

code_info
Lot 04202015:49@1, Expiry date: 5/20/2015; Lot 04272015:06@6, Expiry date: 6/2/2015; Lot 04282015:16@13, Expiry d…Lot 04202015:49@1, Expiry date: 5/20/2015; Lot 04272015:06@6, Expiry date: 6/2/2015; Lot 04282015:16@13, Expiry date: 6/12/2015; Lot 05062015:56@3, Expiry date: 5/24/2015;

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1119-2015%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.