RecallRadar

FDA Drug recall D-1109-2019

PAPAVERINE-PHENTOLAMINE-PGE1 17.44-0.58MG-5.8MCG/ML* INJECTABLE, 5 ml, Professional Compounding Pharmacy, 996 NW Circle Blvd. #105 Corvalli…

On 2019-04-17 the FDA classified a Class II recall of PAPAVERINE-PHENTOLAMINE-PGE1 17.44-0.58MG-5.8MCG/ML* INJECTABLE, 5 ml, Professional Compounding Pharmacy, 996 NW Circle Blvd. #105 Corvalli… by Health Solutions Pharmacy Center, citing lack of Processing Controls: Insanitary conditions observed during compounding of sterile drugs during recent FDA Inspection.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1109-2019
ClassificationClass II
Statusterminated
Initiated2019-02-21
Published2019-04-17
Last updated2026-09-13 11:52 UTC
CompanyHealth Solutions Pharmacy Center
DistributionOR

Product

PAPAVERINE-PHENTOLAMINE-PGE1 17.44-0.58MG-5.8MCG/ML* INJECTABLE, 5 ml, Professional Compounding Pharmacy, 996 NW Circle Blvd. #105 Corvallis, OR 97330 .

Reason

Lack of Processing Controls: Insanitary conditions observed during compounding of sterile drugs during recent FDA Inspection.

Identifiers

code_infoLot:19092018@1, distributed between 09-01-2018 to 02-20-2019.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1109-2019%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.