ICU Medical recalls ChemoLock Port, Bulk, Non-Sterile REF: CL2100-NS due to potential port weld separation causing drug leaks. Affected units have specific UDI and lot numbers.
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
ICU Medical is recalling ChemoLock Port, Bulk, Non-Sterile devices because the port weld may break during use, leading to drug leaks. This could cause serious harm to patients receiving chemotherapy.
The port weld in the device can separate or break while in use, which may cause a leak of chemotherapy drugs. This leak could expose patients to harmful levels of medication, potentially causing serious injury or death.
Patients using chemotherapy with this specific ChemoLock Port device are most at risk. Healthcare providers who administer chemotherapy using these ports may also be affected.
Check for the model number CL2100-NS on the device. Affected units have a unique device identifier (UDI) starting with 00887709094505 and lot number 14407400.
Immediately stop using the ChemoLock Port device if it has the UDI starting with 00887709094505 and lot number 14407400.
The recalled device is ICU Medical ChemoLock Port, Bulk, Non-Sterile REF: CL2100-NS.
Check for the unique device identifier (UDI) starting with 00887709094505 and lot number 14407400 on the device.
Immediately stop using it and contact ICU Medical for further instructions.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0330-2026 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-0330-2026 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.