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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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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Phasitron 5 Breathing Circuits Recalled for Nickel Coating Issue
Percussionaire is recalling Phasitron 5 breathing circuits due to a nickel coating issue that may aerosolize nickel and pose health risks. Customers are advised to dispose of or return affected products, with specific short-term use guidelines for necessary situations.
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GE HealthCare Updates EVair Compressor Recall for Ventilator Use
GE HealthCare has issued an update to the EVair Compressor recall, with testing results confirming safe usage across all patient groups.
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