ICU Medical recalls 30cm IV sets with NanoClave manifold due to potential leaks or separation between 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 leak or separate, causing potential harm during medical use. This recall affects specific batches sold with particular expiration dates.
The NanoClave manifold may develop leaks or separate from the female luer connector during use, potentially causing fluid leakage or interruption of treatment. This could lead to complications for patients receiving IV therapy.
Healthcare professionals using the recalled IV sets are most at risk. Patients receiving treatment with these sets could face complications if a leak or separation occurs.
Check for lot numbers 3303902 or 3380550 on the packaging. The sets expire by August 1, 2021 or December 1, 2021 respectively.
Identify the lot number and expiration date on the packaging to confirm if your set is affected.
Reach out to ICU Medical directly for further assistance or to confirm if your set is part of the recall.
The recall is due to potential leaks or separation between the female luer and NanoClave manifold, which could cause treatment interruptions or complications.
The affected models have lot numbers 3303902 (expires 08/01/2021) or 3380550 (expires 12/01/2021).
Check the lot number on the packaging; affected units have lot numbers 3303902 or 3380550 with specific expiration dates.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2799-2018 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-2799-2018 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.
