Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
84" Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical, Inc. Due to Some devices were labeled as Does not contain...
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 ICU Medical, Inc. directly.
Affected Products
84" Y-Type Blood Set w/170 Micron Filter, Hand Pump, Clave¿, Rotating Luer, Sterile The blood tubing accessory with CLAVE Connector is a single use, sterile, non-pyrogenic device intended for use as an adjunct to blood tubing sets or venipuncture devices for needle-free withdrawal of blood.
Quantity: 160,016 units total
Why Was This Recalled?
Some devices were labeled as Does not contain DEHP even though the product may contain small amounts of DEHP.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About ICU Medical, Inc.
ICU Medical, Inc. has 592 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report