Bard Access Systems: Medical Device Recall in 2013 - (Recall #: Z-0910-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

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.

Product Classification:

Class II

Date Initiated: February 21, 2013

Date Posted: March 13, 2013

Recall Number: Z-0910-2013

Event ID: 64425

Reason for Recall:

Bard Access Systems is recalling two lots of Hickman 9.0 French and one lot of Leonard 10.0 French Dual Lumen Catheters with SureCuff Tissue Ingrowth Cuff with Peel-Apart Percutaneous Introducer Systems due to the wrong size introducer being included with the kit.

Status: Terminated

Product Quantity: 73 units

Code Information:

Lot numbers: HUWI1379 and HUWI1380.

Distribution Pattern:

USA Nationwide Distribution and the countries Europe, Belgium, Australia, and Latin America.

Voluntary or Mandated:

Voluntary: Firm initiated