Fresenius Medical Care Holdings, Inc.: Medical Device Recall in 2020 - (Recall #: Z-1748-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Fresenius 2008T Hemodialysis Machine: Part Number Description 190573 2008T HEMODIAL YSIS SYS. OLC/DIASAFE PLUS; 190713 2008T HEMODIAL YSIS SYS., with CDX; 190766 2008T HEMODIAL YSIS SYSTEM W/BIBAG; 190858 2008T HEMODIAL YSIS SYSTEM WITHOUT CDX; 190895 2008T GEN 2 BIBAG WITHOUT CDX; 190908 2008T HD System With CDX, CAN

Product Classification:

Class II

Date Initiated: March 12, 2020

Date Posted: April 29, 2020

Recall Number: Z-1748-2020

Event ID: 85310

Reason for Recall:

A "Remove USB Device 2" false alarm may be displayed when no USB device or a non-powered USB device is connected to the USB port on the rear of the machine

Status: Ongoing

Product Quantity: 101,463

Code Information:

All serial numbers

Distribution Pattern:

Nationwide Foreign: Canada, Curaca, Guam

Voluntary or Mandated:

Voluntary: Firm initiated