Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

2008T BlueStar Machine Software v.2.72-Hemodialysis machine Model Number: 191126 - Recalled by Fresenius Medical Care Renal Therapies Group, LLC Due to Power Logic Board Fail Message on the 2008T...

Date: April 3, 2019
Company: Fresenius Medical Care Renal Therapies Group, LLC
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Fresenius Medical Care Renal Therapies Group, LLC directly.

Affected Products

2008T BlueStar Machine Software v.2.72-Hemodialysis machine Model Number: 191126 - Product Usage: The 2008T hemodialysis machine is indicated for acute and chronic dialysis therapy in a healthcare facility.

Quantity: 257 units

Why Was This Recalled?

Power Logic Board Fail Message on the 2008T BlueStar Machine with software version 2.72.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Fresenius Medical Care Renal Therapies Group, LLC

Fresenius Medical Care Renal Therapies Group, LLC has 27 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report