Devices

Device Recall Hickman and Leonard Catheters

Model / Serial
Lot numbers: HUWI1379 and HUWI1380.
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
USA Nationwide Distribution and the countries Europe, Belgium, Australia, and Latin America.
Product Description
Leonard 10.0 French Dual Lumen Catheter with SureCuff Tissue Ingrowth Cuff with Peel-Apart Percutaneous Introducer system (product code 0600630). || Product Usage: Hickman and Leonard Catheters are designed for long-term vascular access and for use in patients that lack adequate peripheral venous access.
Manufacturer
Bard Access Systems
2 Events
- Recall of Device Recall Hickman and Leonard Catheters
- Recall of Device Recall Hickman and Leonard Catheters

Manufacturer

Bard Access Systems

Manufacturer Address
Bard Access Systems, 605 North 5600 West, Salt Lake City UT 84116-3738
Manufacturer Parent Company (2017)
Becton, Dickinson and Company
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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