ICU Medical recalls 7.5" (19 cm) Appx 1.5 ml sets with ChemoLock port that may leak if port weld breaks during use. Affected units sold in Canada.
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
ICU Medical is recalling a specific IV set that has a risk of leaking if the port weld breaks during use. This could lead to medication leaks or contamination. Affected units were sold in Canada.
The port weld in the drug transfer device may separate or break during use, potentially causing a leak. This leak could lead to medication contamination or improper dosing if the device is used without the weld being intact.
Healthcare professionals using the ICU Medical 7.5" (19 cm) Appx 1.5 ml set with ChemoLock port in Canada. Patients receiving IV treatments with this specific set are at risk if the port weld fails.
Check for the model number CL3967 on the product. Affected units were distributed in Canada with specific lot numbers: 14369083, 14386090, and 14391965.
Look for the model number CL3967 and the lot numbers 14369083, 14386090, or 14391965 on the product.
The product may have a risk of leaking if the port weld breaks during use, so it is not recommended for use without checking the recall status.
The recall record does not specify a remedy, so no action is required beyond checking if you have the affected model and lot numbers.
This product was distributed in Canada.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0360-2026 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-0360-2026 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.