Fresenius Medical Care Holdings, Inc.: Medical Device Recall in 2020 - (Recall #: Z-1749-2020)

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 BlueStar Hemodialysis Machine Part Number Description: 191124 2008T HD SYS. CDX BLUEST AR; 191126 2008T HD SYS. CDX W/BIBAG BLUEST AR; 191128 2008T HD SYS. W/O CDX BLUEST AR; 191130 2008T HD SYS. W/O CDX W/BIBAG BLUEST AR

Product Classification:

Class II

Date Initiated: March 12, 2020

Date Posted: April 29, 2020

Recall Number: Z-1749-2020

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: 15,342

Code Information:

All serial numbers

Distribution Pattern:

Nationwide Foreign: Canada, Curaca, Guam

Voluntary or Mandated:

Voluntary: Firm initiated