Bard Peripheral Vascular Inc. recalled 14,935 units of the Broviac 4.2 Fr Single-Lumen CV Catheter Tray on December 12, 2025. Damage to the outer tray may compromise the sterile barrier, posing a high hazard. Healthcare providers and patients should stop using the device immediately.
Due to damage to outer tray that can potentially compromise the sterile barrier
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Bard Peripheral Vascular Inc or your healthcare provider for instructions. Notification method: Letter
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The Broviac 4.2 Fr Single-Lumen CV Catheter is used for delivering medications and fluids directly into the bloodstream. It is often used for patients requiring long-term intravenous therapy.
The hazard arises from damage to the outer tray, which can compromise the sterile environment necessary for safe medical use. A breach in sterility can lead to serious infections.
This recall is not part of a broader industry pattern.
Consumers may face health risks if they continue to use the affected catheters, and healthcare providers will need to identify alternative products for their patients.
You can find the catalog number and lot number on the product's packaging or labeling.
Expect a refund processing timeline of approximately 4-6 weeks after returning the product.
Keep copies of all correspondence related to the recall and any receipts or shipping confirmation for returns.
The recalled product is the Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff, Catalog Number 60060. These units were distributed worldwide, including nationwide in the U.S. and in countries like Canada, Australia, and Japan.
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