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Terminated

ChemoSite Low Profile, Implantable Low Profile Mini Catheter Venous Access System with 9 French Introducer Kit with Silicone Catheter Catalog Number: 120025

FDA Recall Z-1093-05 · Posted 2005-08-06

Recalling FirmUnited States Surgical Corporation
Recall StatusTerminated
Product CodeLJS
Date Initiated2005-06-30
Date Terminated2010-09-14
Product Quantity720 units

Reason for Recall

The tear away inroducer sheath may have cracked hubs/handles and /or improper peeling of the sheath during use

Firm Action

United States Surgical notified customers by letter dated June 30, 2005 requesting return of the recalled product.

Root Cause

Other

Distribution Pattern

Nationwide Foreign: Australia, Canada, Germany,Israel, Uruguay, Chile,

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K902135PERCUTANEOUS INTRODUCER KITDevice Labs, Inc. · 1990-08-01

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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