Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
9F Plastic Dual Port Recalled by Medical Components, Inc dba MedComp Due to The dual port with catheters was not covered...
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 Medical Components, Inc dba MedComp directly.
Affected Products
9F Plastic Dual Port; The port systems are totally implantable vascular access devices. They consist of an injection port, a self-sealing membrane and a detachable catheter. The port systems provide repeated vascular access and are applicable for delivery of: medications, intravenous fluids, blood products, parenteral nutrition, and for venous blood sampling.
Quantity: 325
Why Was This Recalled?
The dual port with catheters was not covered under FDA clearance.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medical Components, Inc dba MedComp
Medical Components, Inc dba MedComp has 38 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report