Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
2008T HD SYS. W/O CDX BLUESTAR Recalled by Fresenius Medical Care Holdings, Inc. Due to Potential PCBA leaching from tubing of hemodialysis machines.
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 Holdings, Inc. directly.
Affected Products
2008T HD SYS. W/O CDX BLUESTAR
Quantity: 733 units
Why Was This Recalled?
Potential PCBA leaching from tubing of hemodialysis machines.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Fresenius Medical Care Holdings, Inc.
Fresenius Medical Care Holdings, Inc. has 161 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report