Smiths Medical Recalls Endotracheal Tubes Over Ventilation Risk
Devices are being removed from use after certain sizes were found to have smaller diameters than expected, potentially limiting airflow. Eight injuries have been reported.
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BD Issues Correction for Infusion Pump Software
BD is correcting software for its Alaris Systems Manager and CCE Infusion Adapter after identifying a risk that outdated infusion parameters could be uploaded, potentially leading to incorrect dosing.
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FDA Issues Early Alert on Baxter Spectrum Infusion Pump Recall
The FDA has issued an early alert regarding Baxter’s recall of certain Spectrum infusion pumps due to missing motor mounting screws, which may have occurred during servicing.
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Medical Device Recalls Reach Highest Level in Four Years
Sedgwick brand protection releases a year-in-review analysis of 2024 recall data, including the top five failures for medical devices.
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Abiomed Updates Use Instructions for Impella RP Pumps Due to Device Interaction Risk
Abiomed has updated the use instructions for its Impella RP pumps due to a risk of device interaction that could damage the optical sensor or temporarily stop the pump.
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