CareFusion recalls Alaris EtCO2 Module Model 8300 infusion pumps due to potential bent connectors that could delay infusion starts. Affected units have specific serial numbers and UDI-DI codes.
Due to affected devices that may have bent female IUI connector and may not be operable and potentially cause delays in the start of the infusion or monitoring.
CareFusion is recalling Alaris EtCO2 Module Model 8300 infusion pumps because some units may have a bent connector that could cause delays in starting infusions or monitoring. This could affect medical treatment timing for patients using the device.
The device may have a bent female IUI connector that prevents proper operation. This could cause delays in starting infusions or monitoring, potentially affecting treatment timing. However, the hazard does not indicate immediate injury risks.
Healthcare professionals using the Alaris EtCO2 Module Model 8300 for infusion monitoring. Patients receiving treatments through this system may be at risk if the device malfunctions.
Check for serial numbers starting with 16233 or 16192, or UDI-DI codes 10885403830020 and 10885403830013. The product is a modular infusion pump and monitoring system.
Look for serial numbers listed in the recall notice (e.g., 16233040, 16233078, etc.) to confirm if your unit is affected.
The recall is due to affected devices that may have a bent female IUI connector, which could cause delays in starting infusions or monitoring.
Check your device's serial number against the list provided in the recall notice (e.g., 16233040, 16233078, etc.).
The recall does not require immediate stoppage; affected units may still function but could cause delays in treatment.
We’ve drafted a message you can send CareFusion to request your refund or repair — edit it as you like.
Subject: Recall Z-3140-2024 — CareFusion CareFusion Hello, I own a CareFusion that is covered by recall Z-3140-2024 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.
