RecallRadar

FDA Drug recall D-1123-2015

Hyaluronidase (RM ONLY), Injectable Solution, 150 U/mL, 10ML vial, Rx only, compounded by Montana Compounding Pharmacy, Missoula, MT

On 2015-06-17 the FDA classified a Class II recall of Hyaluronidase (RM ONLY), Injectable Solution, 150 U/mL, 10ML vial, 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-1123-2015
ClassificationClass II
Statusterminated
Initiated2015-05-15
Published2015-06-17
Last updated2026-09-13 11:51 UTC
CompanyMontana Compounding Pharmacy
DistributionMT, ND

Product

Hyaluronidase (RM ONLY), Injectable Solution, 150 U/mL, 10ML vial, 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 02062015:06@3, expiry date: 5/17/2015; Lot 02272015:93@1, expiry date: 6/30/2015; Lot 03252015:92@7, expiry date:…Lot 02062015:06@3, expiry date: 5/17/2015; Lot 02272015:93@1, expiry date: 6/30/2015; Lot 03252015:92@7, expiry date: 6/30/2015; Lot 04162015:63@7, expiry date: 6/30/2015.

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-1123-2015%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.