Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PowerPort isp M.R.I. Implantable Port with Attachable 8F Polyurethane Open-Ended Recalled by Bard Peripheral Vascular Inc Due to Complaints received that products packaged with the incorrect...
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 Peripheral Vascular Inc directly.
Affected Products
PowerPort isp M.R.I. Implantable Port with Attachable 8F Polyurethane Open-Ended Single-Lumen Venous Catheter
Quantity: 900 units
Why Was This Recalled?
Complaints received that products packaged with the incorrect introducer sheath size.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Bard Peripheral Vascular Inc
Bard Peripheral Vascular Inc has 136 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report