Release date: 2014-04-24
The US Food and Drug Administration issued an emergency warning that ARKON anesthesia equipment manufactured by Spacelabs Healthcare in the UK was found to have serious software defects that could lead to life-threatening failures. ARKON's anesthesia system was used by hospitals to provide oxygen, anesthetic gas and nitrous oxide to patients during surgery. Spacelabs announced the recall of the device last month.
The version 2.0 software running on the device was found to have serious bugs that could cause the device to stop working and require patient hand-controlled ventilation. In addition, the device has 4 USB ports, but if the phone or other USB device is plugged in, it may cause the device to stop working. This bug can lead to serious consequences, including death and hypoxemia.
Source: Chinese Industry Information Station
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