Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MRCTT80041 MedComp 8F Plastic Pro-Fuse(R) CT Low Profile Port with Recalled by Medical Components, Inc dba MedComp Due to Product was packaged with the incorrect port and...
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
MRCTT80041 MedComp 8F Plastic Pro-Fuse(R) CT Low Profile Port with Attachable Chronoflex(R) Polyurethane Catheter. Power Injectable Implantable Infusion Port insertion kit.
Quantity: 30
Why Was This Recalled?
Product was packaged with the incorrect port and does not match the label. The kit is labeled as an 8F Low Profile Pro-Fuse CT Port. The kit contains an 8F Midsize Dignity CT Port.
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