Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
168 cm (66") Appx 2.6 ml Recalled by ICU Medical, Inc. Due to The connection between the Female Luer and the...
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
168 cm (66") Appx 2.6 ml, PVC/PUR Smallbore Ext Set w/6-Port NanoClave¿ Manifold, Check Valve, MicroClave¿ Clear, Rotating Luer. Product Usage: The device is a single use, sterile, non-pyrogenic device which provides access for the administration of fluids from a container to a patients vascular system through the administration sets needle or catheter (which is inserted into a vein).
Quantity: 120 units
Why Was This Recalled?
The connection between the Female Luer and the NanoClave¿ manifold has the potential for developing a leak.
Where Was This Sold?
This product was distributed to 4 states: AZ, OH, TX, WA
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