Health product recall

Hickman™ and Broviac™ Central Venous Catheter Kits

Last updated

Summary

Product
Hickman™ and Broviac™ Central Venous Catheter Kits
Issue
Medical devices - Sterility
What to do

Contact the manufacturer if you require additional information.

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalogue number

Hickman Dual-Lumen CV Catheter With SureCuff Tissue Ingrowth Cuff

More than 10 numbers, contact manufacturer.

0600350

Hickman Dual-Lumen CV Catheter With SureCuff Tissue Ingrowth Cuff

More than 10 numbers, contact manufacturer.

0600570

Hickman Dual-Lumen CV Catheter With SureCuff Tissue Ingrowth Cuff

More than 10 numbers, contact manufacturer.

0600620

Broviac 6.6 Fr Single-Lumen CV Catheter Peel-Apart Introducer Kit With SureCuff Tissue Ingrowth Cuff

HUKR0065

0600540

Broviac 6.6 Fr Single-Lumen CV Catheter Peel-Apart Introducer Kit With SureCuff Tissue Ingrowth Cuff

HUKU0279

0600540

Broviac 6.6 Fr Single-Lumen CV Catheter Peel-Apart Introducer Kit With SureCuff Tissue Ingrowth Cuff

HUKU0270

0600540

Hickman 12.5 Fr Triple-Lumen CV Catheter, Peel-Apart Introducer Kit With SureCuff Tissue Ingrowth Cuff

HUKQ0535

0600650

Hickman 9.6 Fr Single-Lumen CV Catheter, Peel-Apart Introducer Kit With SureCuff Tissue Ingrowth Cuff

HUKU0311

0600560

Hickman 9.6 Fr Single-Lumen CV Catheter, Peel-Apart Introducer Kit With SureCuff Tissue Ingrowth Cuff

HUKS0776

0600560

Issue

BD has identified via internal inspections that the packaging of some Hickman catheter and Broviac catheter kits may have damage present on the outer tray, potentially compromising the sterile barrier. This product features a double-tray packaging structure (outer tray and inner tray). The inner tray, which contains the catheter and accessories, is sealed inside the outer tray along with the instructions for use. The sterility of the outer surface of the inner tray and the instructions for use may be compromised.

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Health products - Medical devices - General hospital and personal use
Companies
Bard Access Systems, Inc.
605 North 5600 West, Salt Lake City, Utah, United States, 84116
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Recall date
Identification number
RA-81509

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