ICU Medical recalls 75-inch IV sets with NanoClave manifold due to potential leak or separation between female luer and manifold. Affected units have specific lot numbers and expiration dates.
ICU Medical is expanding the scope of their previously initiated recall to include additional I.V. Administration Sets with NanoClave manifold due to the potential to develop a leak or for separation between the female luer and the NanoClave manifold.
ICU Medical is recalling certain IV administration sets that may separate or leak between the female luer and NanoClave manifold. This could lead to improper fluid delivery during medical procedures.
The female luer connector may separate from the NanoClave manifold, causing leaks or improper fluid flow. This could lead to incorrect medication dosing or infection risks during IV treatments.
Healthcare professionals using these IV sets in medical facilities are most at risk. Patients receiving IV treatments with the recalled sets could face complications.
Check for the item number 011-AM6125 on the packaging. Affected units have lot number 3424313 and expire by March 1, 2022.
Look for item number 011-AM6125 on the packaging with lot number 3424313 and expiration date 03/01/2022.
The recall is due to potential separation between the female luer and NanoClave manifold, which could cause leaks or improper fluid flow during IV treatments.
Check the item number and lot number on the packaging. If it matches the recalled units, contact ICU Medical for guidance.
The recall addresses potential separation or leaks that could lead to incorrect medication dosing or infection risks, but the remedy does not specify immediate action to stop use.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2807-2018 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-2807-2018 from ICU Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
