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FDADecember 12, 2025device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Ongoing

Brands named

bard peripheral vascularbardbard peripheral

UPCs

008017410516920080174105170800801741051715008017410517390080174105177700801741051807008017410518210080174105184500801741051869008017410519130080174105197500801741052019

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff Cat 60060 — Recall Details · AllClear