ICU Medical recalls 73" (185 cm) Appx 2.5 ml Ext Set with ChemoLock Port due to potential port leak from weld separation during use. Affected units have UDI:10887709123356/Lot:14332784.
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 may leak if the port weld breaks during use. This could lead to medication leaks or contamination. Affected units have a unique identifier and lot number.
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 not addressed.
Healthcare professionals using the ICU Medical 73" Appx 2.5 ml Ext Set with ChemoLock Port are most at risk. Patients receiving IV treatments with this device may also be affected.
Check for the product name: ICU Medical 73" (185 cm) Appx 2.5 ml Ext Set with ChemoLock Port, Clamp, and ChemoLock w/Red Cap. Affected units have UDI:10887709123356 and Lot:14332784.
Verify the unique device identifier (UDI) and lot number on the product label.
The recall states the port weld may separate or break during use, potentially causing a leak. This could lead to medication contamination or improper dosing.
Check for the product name: ICU Medical 73" (185 cm) Appx 2.5 ml Ext Set with ChemoLock Port, Clamp, and ChemoLock w/Red Cap. Affected units have UDI:10887709123356 and Lot:14332784.
The recall does not specify a remedy, so check the product details and contact ICU Medical if you have concerns.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0340-2026 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-0340-2026 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.
