ICU Medical recalls 10" Smallbore 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 10" Smallbore IV sets with NanoClave manifolds because they might leak or separate, causing safety issues during medical use. This recall affects specific lot numbers and expiration dates.
The NanoClave manifold can develop leaks or separate from the female luer during use, which may lead to improper fluid delivery or contamination. This poses a risk of infection or treatment errors in medical settings.
Healthcare professionals using these IV sets in medical facilities are most at risk. Patients receiving IV treatments with the recalled sets could face complications if the set separates or leaks.
Check for lot numbers 3373758, 3391364, or 3511445 on the product label. The expiration dates are 12/01/2021, 01/01/2022, or 08/01/2022 respectively.
Look for lot numbers 3373758, 3391364, or 3511445 and expiration dates 12/01/2021, 01/01/2022, or 08/01/2022.
The recall is due to potential leaks or separation between the female luer and NanoClave manifold, which could cause treatment errors or infections.
Check the product label for the lot numbers and expiration dates listed. If you have the affected units, contact ICU Medical for further instructions.
Yes, separation could lead to improper fluid delivery or contamination, posing a risk of infection or treatment errors in medical settings.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2813-2018 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-2813-2018 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.
