Medical Components, Inc dba MedComp: Medical Device Recall in 2012 - (Recall #: Z-1868-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

MRCTT80041 MedComp 8F Plastic Pro-Fuse(R) CT Low Profile Port with Attachable Chronoflex(R) Polyurethane Catheter. Power Injectable Implantable Infusion Port insertion kit.

Product Classification:

Class II

Date Initiated: April 2, 2012

Date Posted: July 4, 2012

Recall Number: Z-1868-2012

Event ID: 62238

Reason for Recall:

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.

Status: Terminated

Product Quantity: 30

Code Information:

Catalog number MRCTT80041, Lot # MDNK860, Exp 02/2015

Distribution Pattern:

Worldwide Distribution-USA (nationwide) including the states of GA and WA and the countries of Ireland and Turkey.

Voluntary or Mandated:

Voluntary: Firm initiated