CareFusion recalls all Pyxis CII Safe ES Tower Main units (REF: 111:00) due to potential fluid ingress causing smoke, system downtime, or fire. Affected units have specific serial numbers.
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
CareFusion is recalling all Pyxis CII Safe ES Tower Main units with serial numbers starting with 1116-00. This could lead to smoke, system shutdowns, or fires if fluid enters the anesthesia or med stations.
Fluid entering the anesthesia or med stations could cause smoke, system shutdowns, or fires. This happens due to a design flaw that allows liquids to seep into the device's internal components.
Healthcare facilities using the Pyxis CII Safe ES Tower Main for anesthesia or medication delivery are most at risk. Patients and staff could be affected if the device malfunctions.
Check for the serial number starting with 1116-00 on the Pyxis CII Safe ES Tower Main. The product was sold with reference number 1116-00 and serial number 10885403512605.
Inspect the device for signs of fluid leakage or damage to the anesthesia or med stations.
The product is the Pyxis CII Safe ES Tower Main with serial numbers starting with 1116-00.
The recall record does not mention a remedy or fix.
Check for the serial number starting with 1116-00 on the Pyxis CII Safe ES Tower Main.
We’ve drafted a message you can send CareFusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0371-2026 — CareFusion CareFusion Hello, I own a CareFusion that is covered by recall Z-0371-2026 from CareFusion. 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.