ICU Medical recalls 30" admin sets with potential port leaks. Stop using if port may break during use.
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
ICU Medical is recalling 30-inch admin sets that may have a port weld that breaks, causing leaks. This could lead to medication leaks or contamination if the device is used.
The port weld in the drug transfer device may separate or break during use, leading to leaks. This could cause medication to leak out of the system, potentially contaminating the patient or causing adverse reactions.
Healthcare professionals using these admin sets for chemotherapy or medication delivery. Patients receiving treatment through these devices are at risk if the port breaks.
Check for the model: ICU Medical 30" (76 cm) Appx 3.6 ml, 20 Drop Admin Set with ChemoLock w/Red Cap. The product has a reference number CL3511 and lot number 14400616.
Inspect the port for signs of separation or damage that could cause leaks.
Reach out to ICU Medical for further assistance or to confirm if your device is affected.
The recall indicates the port weld may break during use, so it is not safe to use without checking for leaks.
Check for leaks and contact ICU Medical for further instructions.
Look for the model: ICU Medical 30" (76 cm) Appx 3.6 ml, 20 Drop Admin Set with ChemoLock w/Red Cap. The product has a reference number CL3511 and lot number 14400616.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0333-2026 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-0333-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
