DEVICE WARNING: Baxter Healthcare Corporation Recalls SIGMA Spectrum Infusion Pumps with Master Drug Library and Spectrum IQ Infusion Systems with Dose IQ Safety Software for Repeat Upstream Occlusion False Alarms
Impact Level:
Moderate
Source: FDA MedWatch
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DEVICE WARNING: GE HealthCare Recalls TruSignal SpO2 Sensors for Issues That May Reduce Defibrillation Energy, Expose Patients to Unintended Voltage, or Give Inaccurate Readings
Impact Level:
Moderate
Source: FDA MedWatch
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DEVICE CAUTIONARY NOTICE: Recalled: Hamilton C1, C2, C3 & T1 Ventilators Due to a Software Anomaly That May Cause it to Stop and Enter Ambient Mode
Impact Level:
Low
Source: FDA Medical Device Recalls
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DEVICE WARNING: MEGADYNE Suction Coagulators Recalled: Product issue may lead to fluid ingress into handpiece
Impact Level:
Moderate
Source: FDA Medical Device Recalls
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The North American Spine Society is committed to quality patient care through promotion of patient safety and prevention of medical errors. NASS monitors a variety of government and other resources for patient safety-related notices that may be useful to our members. Information from these notices is also archived on the NASS website and can be viewed by clicking here. This information is provided as a service for information and education only.