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Recall Observatory FDA recall evidence

Device product

2008T and 2008TBluestar Hemodialysis Machines with CDX-Indicated for acute and chronic dialysis therapy in a healthcare facility Models: (1) 190713 2008T HEMODIALYSIS SYS., with CDX; (2) 190766 2008T HEMODIALYSIS SYSTEM W/BIBAG W/CDX ; (3) 191124 2008T HD SYS. CDX BLUESTAR; (4) 191126 2008T HD SYS. CDX W/BIBAG BLUESTAR

Z-0734-2023

July 27, 2022

Class II

Product summary

Firm
Fresenius Medical Care Holdings, Inc.
Event
Event 91154
Status
Ongoing
Classification
Class II
Quantity
2008T with CDX= 70,552 2008T Bluestar with CDX= 25,205
Official record key
device-enforcement:Z-0734-2023

Official wording

Reason: (1)Software version 2.74 upgrade and (2)hardware related cause that affects only CDX Machines, has been identified as the UI-MICs Board is sensitive to Electromagnetic Interference (EMI) which will cause the false alarm "Remove USB 2 Device".

Code information: Software issue in SW versions 2.72 and earlier with CDX. UDI: (1) 00840861100897; (2) 00840861100910; (3) 00840861102082; (4) 00840861102099

Distribution pattern: US Nationwide distribution.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    Software version 2.74 upgrade and (2)hardware related cause