Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Trifurcated Transpac IT Monitoring Kit w/03 ml Flush Devices Recalled by ICU Medical, Inc. Due to ICU has become aware of an issue with...
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
Trifurcated Transpac IT Monitoring Kit w/03 ml Flush Devices, Needleless Valve and Macrodrip, Item No. 011-46104-33 Transpac Trifurcated monitoring kit with Safeset Reservoir, squeeze flush and sampling ports. The monitoring kit is intended for measuring and montoring of fluid pressure, fluid infusion, and blood withdrawal.
Quantity: 40 units
Why Was This Recalled?
ICU has become aware of an issue with a component where the connection on an arterial monitoring kit may crack and cause a fluid leak.
Where Was This Sold?
Worldwide Distribution - USA including Oregon and Internationally to Australia.
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