Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PowerPort Slim Implantable Port Recalled by Bard Access Systems Due to Labeling discrepancy.The label states that the implantable port...
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 directly.
Affected Products
PowerPort Slim Implantable Port, indicated for patient therapies requiring repeated access to the vascular system. Product Codes: 1716000, 1716070
Quantity: 777
Why Was This Recalled?
Labeling discrepancy.The label states that the implantable port contains silicone suture plugs, however approximately 23% of the units contained in the affected lots have a PowerPort Slim titanium implantable port without silicone suture plugs.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Bard Access Systems
Bard Access Systems has 24 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report