Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PowerPICC Provena Catheters Recalled by Bard Access Systems Inc. Due to Possible leaks on the 3 Fr. Single lumen...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Bard Access Systems Inc. directly.
Affected Products
PowerPICC Provena Catheters, as 3 Fr. Single lumen and 4 Fr. Dual Lumen. Packaged in a poly tray with Tyvek lid within a header bag configuration or a breather bag configuration.
Quantity: 53,699 units total
Why Was This Recalled?
Possible leaks on the 3 Fr. Single lumen and 4 Fr. Dual lumen PowerPICC catheters at the luer hub extension leg junction.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Bard Access Systems Inc.
Bard Access Systems Inc. has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report