Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0909-2013 — Hickman 9.0 French Dual Lumen Catheter with SureCuff Tissue Ingrowth Cuff with Peel-Apart Percutaneous Introducer system (pediatric product code 0600580; adult product code 0600600). Product Usage: Hickman and Leonard Catheters are designed for long-term vascular access and for use in patients th

U.S. FDA — Device Enforcement · United States · 2013-02-21 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0909-2013
Date of alert: 2013-02-21
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Bard Access Systems
Product category: device
Product type: Devices

Reported risk: 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.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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