CareFusion recalls Alaris EtCO2 Module Model 8300 due to dim LED display segments. Affected units have serial numbers; no remedy specified in official notice.
LED display, which provides infusion or patient monitoring values, on the module may have segments that appear dim.
CareFusion is recalling Alaris EtCO2 Module Model 8300 devices because their LED display may show dim segments. This issue doesn't affect patient safety but could cause confusion in monitoring readings.
The LED display segments may appear dim, potentially causing confusion about infusion or patient monitoring values. However, this does not pose a direct safety risk to patients or users.
Healthcare caregivers using the Alaris EtCO2 Module Model 8300 for infusion monitoring. Those with the device and serial numbers are most at risk.
Check if your device has the Alaris EtCO2 Module Model 8300 name and a serial number. The product is used by healthcare caregivers for automated infusion programming.
Verify your Alaris EtCO2 Module Model 8300 has a serial number for identification.
No, the dim LED display does not pose a safety risk but could cause confusion in monitoring readings.
The official notice does not specify a remedy, so no action is required beyond checking the serial number.
Affected units have the Alaris EtCO2 Module Model 8300 name and a serial number.
We’ve drafted a message you can send CareFusion to request your refund or repair — edit it as you like.
Subject: Recall Z-2825-2020 — CareFusion CareFusion Hello, I own a CareFusion that is covered by recall Z-2825-2020 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.