ICU Medical recalls Oncology Kit with ChemoLock Port REF: CL4136 due to potential port weld separation causing leaks. Affected units have UDI:10887709096131/Lot:14393176.
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
ICU Medical is recalling its Oncology Kit with ChemoLock Port (REF: CL4136) because the port weld might break during use, leading to leaks. This could cause medication exposure or contamination risks for patients and healthcare workers.
The port weld in the drug transfer device can separate or break during use, which may cause a leak of chemotherapy medication. This leak could expose healthcare workers to hazardous chemicals or contaminate the patient's treatment area.
Healthcare professionals using the ChemoLock Port kit are most at risk, particularly those handling chemotherapy treatments. Patients receiving care through this port may also be affected if leaks occur.
Check for the ChemoLock Port with REF: CL4136. Affected units have a Unique Device Identifier (UDI): 10887709096131 and Lot number: 14393176.
Inspect the port weld for signs of separation or damage that could cause leaks.
Reach out to ICU Medical directly for guidance on next steps if leaks are suspected.
The recall primarily affects healthcare professionals using the kit. Patients receiving treatment through this port may be at risk if leaks occur.
Check for the ChemoLock Port with REF: CL4136. Affected units have UDI: 10887709096131 and Lot number: 14393176.
Contact ICU Medical directly for guidance on next steps if leaks are suspected.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0336-2026 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-0336-2026 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.
