ICU Medical recalls 50 pouches of NanoClave T-Connectors due to potential seal failure with spikes. Affected units have specific UDI codes. Stop using immediately to prevent improper sealing.
Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lots of NanoClave sets, which may inhibit a proper seal with the NanoClave spike.
ICU Medical is recalling 50 pouches of NanoClave T-Connectors because a manufacturing defect might prevent proper sealing with the spike. This could lead to improper connections during medical procedures.
The internal surface of the NanoClave T-Connector may have a manufacturing defect that prevents it from sealing properly with the spike. This could lead to improper connections during medical procedures, potentially causing leaks or other complications.
Healthcare professionals using the NanoClave T-Connectors for intravascular administration sets. Those with the specific UDI code (01)10887709040141(17)250101(30)25(10)4573652 are most at risk.
Check for the UDI code (01)10887709040141(17)250101(30)25(10)4573652 on the packaging. The product includes 1 unit per pouch, 50 pouches per case.
Discard the affected NanoClave T-Connectors to prevent potential improper sealing during medical procedures.
The UDI code for the recalled units is (01)10887709040141(17)250101(30)25(10)4573652.
50 pouches of NanoClave T-Connectors are affected.
A potential manufacturing defect on the internal surface of the NanoClave T-Connector may inhibit a proper seal with the spike.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0252-2021 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-0252-2021 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.
