ICU Medical recalls Chemo Lock Universal Vented V:10 vial spikes due to potential port weld separation causing drug leaks. Affected units have UDI 00887709070981 and lot 14380109.
Port weld of drug transfer device may separate or break during use and potentially result in a leak.
ICU Medical is recalling Chemo Lock Universal Vented Vial Spikes REF: CL-70-10 because the port weld may break during use, causing drug leaks. This could lead to medication exposure or contamination risks for patients.
The port weld that connects the vial spike to the drug container may separate or break during use. This can cause medication to leak, potentially exposing healthcare workers or patients to harmful substances.
Healthcare professionals using the Chemo Lock vial spikes for chemotherapy treatments are most at risk. Patients receiving chemotherapy through these devices could also be affected if the spike leaks.
Check for the product name 'Chemo Lock Universal Vented Vial Spike' with reference number CL-70-10. Affected units have a unique device identifier (UDI) of 00887709070981 and lot number 14380109.
Verify the product name and reference number on the device to confirm it matches the recalled Chemo Lock Universal Vented Vial Spike REF: CL-70-10.
Reach out to ICU Medical directly for guidance on next steps if you have the recalled product.
The recall states the port weld may separate or break during use, potentially causing drug leaks. This could lead to medication exposure risks, but the remedy does not specify immediate stop-use.
Check for the product name 'Chemo Lock Universal Vented Vial Spike' with reference number CL-70-10. Affected units have a unique device identifier (UDI) of 00887709070981 and lot number 14380109.
The recall does not specify a remedy, so contact ICU Medical directly for guidance on next steps.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0329-2026 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-0329-2026 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.
