Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Hemodialysis System Recalled by Nipro Medical Corporation Due to Screw may loosen or fallout of Hemodialysis system
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 Nipro Medical Corporation directly.
Affected Products
Hemodialysis System, Surdial DX REF: MC+SDX01 Rx Only
Quantity: N/A
Why Was This Recalled?
Screw may loosen or fallout of Hemodialysis system
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Nipro Medical Corporation
Nipro Medical Corporation has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report