Medical Components, Inc dba MedComp: Medical Device Recall in 2015 - (Recall #: Z-1527-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: January 28, 2015

Date Posted: May 6, 2015

Recall Number: Z-1527-2015

Event ID: 70457

Reason for Recall:

The dual port with catheters was not covered under FDA clearance.

Status: Terminated

Product Quantity: 325

Code Information:

Model No. MR592090A, MR592090P; with Lot Nos.: MAKT120 EXP. DATE 04/28/2012, MAXH410 EXP. DATE 06/28/2014, MAXF610 EXP. DATE 10/28/2014, MBFC140 EXP. DATE 05/28/2016, MBGH020 EXP. DATE 08/28/2016, MBHS100 EXP. DATE 11/28/2016, MAKT130 EXP. DATE 04/28/2012, MBAQ860 EXP. DATE 07/28/2015, MBHP980 EXP. DATE 11/28/2016, MBKJ110 EXP. DATE 03/28/2017

Distribution Pattern:

Worldwide distribution. US nationwide, Canada, Brazil, and United Arab Emirates.

Voluntary or Mandated:

Voluntary: Firm initiated