RecalledThisWeek Search
Medium risk Medical DevicesClass II

Broviac 4.2 Fr Catheter Cutdown Tray Recall

Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff Cat 60060

Updated December 12, 2025

Bard Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff (Cat 60060) is being recalled due to potential damage to the outer tray that can compromise the sterile barrier. This damage could expose the catheter to contamination.

Is the Bard Peripheral Vascular Inc recalled? Yes. This product was recalled by FDA on December 12, 2025. Details below.

What is recalled

Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff, Catalog number 60060, manufactured by Bard Peripheral Vascular Inc.

Am I affected

You're affected if you have a Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff with catalog number 60060. Check the product packaging and labeling for the catalog number.

What to do right now

Stop using this product immediately. Contact Bard Peripheral Vascular Inc or the facility that supplied the catheter tray to arrange for a replacement or proper handling instructions.

The hazard

Due to damage to outer tray that can potentially compromise the sterile barrier

Brands affected

Bard Peripheral Vascular Inc
Source
FDA
Category
Medical Devices
Recall ID
fda-Z-1367-2026
Classification
Class II
Recalled
December 12, 2025
Read the official notice

Get free recall alerts

New Medical Devices recalls, the moment they post.

Free forever. Unsubscribe anytime. We never sell your data.

More Medical Devices recalls