Devices

Device Recall Proplege Coronary Sinus Catheter

Model / Serial
Model PR9, lot numbers: 59385159, 59385164, 59385204, 59398000, 59398006, 59398008, 59400402, 59423199, 59423200, 59385159, 59385164, 59385204, 59398000, 59398006.
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution - USA Nationwide including the states of: MD, NY, PA, CA, FL, AZ, AL, TX, VA, OH, MO, NC, GA, TN, CO, OR, SC, ME, IL, HI, NJ, WA, WI, CT, KY, LA and Canada.
Product Description
Proplege Coronary Sinus Catheter model PR9, 11 French Introducer, kitted with PR9. || Product Usage: The catheter introducer sheath kit provides access to the central venous circulation to facilitate catheter and guidewire insertion. The Proplege coronary sinus catheter provides retrograde cardioplegia during cardiopulmonary by-pass surgery.
Manufacturer
Edwards Lifesciences, LLC
1 Event
- Recall of Device Recall Proplege Coronary Sinus Catheter

Manufacturer

Edwards Lifesciences, LLC

Manufacturer Address
Edwards Lifesciences, LLC, 12050 Lone Peak Pkwy, Draper UT 84020-9414
Manufacturer Parent Company (2017)
Edwards Lifesciences Corporation
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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