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
- Source
- FDA
- Category
- Medical Devices
- Recall ID
- fda-Z-1367-2026
- Classification
- Class II
- Recalled
- December 12, 2025
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