ICU Medical recalls IV sets with NanoClave manifold due to potential leaks or separation between the 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 IV administration sets with NanoClave manifold because they may leak or separate, causing potential injury. This affects specific lot numbers and expiration dates.
The NanoClave manifold may leak or separate from the female luer connector, potentially causing injury during IV administration. This risk occurs when the sets are used normally without proper attachment.
Healthcare professionals using IV sets with NanoClave manifold are most at risk. Patients receiving IV treatments with these sets could be affected.
Check for lot numbers 3393136 or 3508527 on the packaging. The expiration dates are November 1, 2022, or August 1, 2022, respectively.
Look for lot numbers 3393136 or 3508527 on the packaging of the IV sets.
Reach out to ICU Medical for further assistance if you have the affected lot numbers.
The NanoClave manifold may leak or separate from the female luer connector, potentially causing injury during IV administration.
Lot numbers 3393136 and 3508527 are affected, with expiration dates of November 1, 2022, and August 1, 2022, respectively.
No, but you should check the lot numbers and contact ICU Medical if you have affected units.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2806-2018 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-2806-2018 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.
