ICU Medical recalls oncology kits with potential port leaks. Stop using if port weld may break during chemotherapy administration.
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
ICU Medical is recalling oncology kits that may have a port weld that breaks during use, causing leaks. This could lead to medication exposure risks for patients and healthcare workers.
The port weld in the drug transfer device may separate or break during use, potentially causing a leak of chemotherapy medication. This leak could expose healthcare workers and patients to harmful substances.
Healthcare professionals using the recalled oncology kits for chemotherapy administration are most at risk. Patients receiving treatment with these kits could also be affected.
Check for the product name: ICU Medical Oncology Kit with 31" (7.9 cm) 20 Drop Admin Set and ChemoLock Port Drip Chamber. The lot numbers 14400216 and 14416769 are associated with this recall.
Verify the lot numbers 14400216 or 14416769 on the product label.
If the port weld appears damaged or the product is from the recalled lot numbers, stop using it immediately.
The port weld in the drug transfer device may separate or break during use, potentially causing a leak of chemotherapy medication.
Check for the product name: ICU Medical Oncology Kit with 31" (79 cm) 20 Drop Admin Set and ChemoLock Port Drip Chamber. The lot numbers 14400216 and 14416769 are associated with this recall.
If the port weld appears damaged or the product is from the recalled lot numbers, stop using it immediately. 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-0334-2026 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-0334-2026 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.
