Fresenius recalls 2008T BlueStar hemodialysis machines with specific part numbers due to false USB device alerts when no device is connected. Affected units may display a 'Remove USB Device 2' message unnecessarily.
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
Fresenius is recalling certain 2008T BlueStar hemodialysis machines because they may show a false 'Remove USB Device 2' alert when no USB device is connected. This does not cause harm but could confuse users about device connections.
The machine may display a 'Remove USB Device 2' alert even when no USB device is connected or when the device is unplugged. This false alarm does not cause physical harm but could lead to unnecessary confusion about device connections.
Patients using Fresenius 2008T BlueStar hemodialysis machines with part numbers 191124, 191126, 191128, or 191130 are affected. Healthcare providers managing these machines are most at risk of confusion.
Check for part numbers 191124, 191126, 191128, or 191130 on the machine's label. All units with these part numbers are affected, regardless of serial number.
Look for the 'Remove USB Device 2' message appearing when no USB device is connected to the machine.
No, the recall does not require stopping use. The false alert is not harmful but may cause confusion.
Part numbers 191124, 191126, 191128, and 191130 are affected.
The recall does not provide a fix; users should monitor for the false alert and ensure proper USB connections.
We’ve drafted a message you can send Fresenius to request your refund or repair — edit it as you like.
Subject: Recall Z-1749-2020 — Fresenius Fresenius Hello, I own a Fresenius that is covered by recall Z-1749-2020 from Fresenius. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
