MR 5300, Magnetic Resonance System.
Philips North America
Patient support table floor plate may be incorrectly installed.
π₯ Medical Devices β’ 15,809 recalls
Philips North America
Patient support table floor plate may be incorrectly installed.
Philips North America
Patient support table floor plate may be incorrectly installed.
Philips North America
Patient support table floor plate may be incorrectly installed.
Philips North America
Patient support table floor plate may be incorrectly installed.
The blood cultures performed as part of the organ donation process were positive for Staphylococcus aureus.
Philips North America
Patient support table floor plate may be incorrectly installed.
Philips North America
Patient support table floor plate may be incorrectly installed.
Draeger Medical
Unexpected shutdown while operating on battery power.
Degraded and unusable upon removal from the foil pouch due to exposed environmental conditions during transit and storage, compromising sterility
Philips North America
Patient support table floor plate may be incorrectly installed.
Philips North America
Patient support table floor plate may be incorrectly installed.
Philips North America
Patient support table floor plate may be incorrectly installed.
Philips North America
Patient support table floor plate may be incorrectly installed.
Retrospective engineering analysis against current ISO standards for hoists has determined: 1. The device cannot physically perform at maximum documented weight specifications when a factor of safety of two times the maximum load is applied. 2. The device is not equipped with a safety device to ensure a person with disability would not fall in the event of a single-fault condition of the lifting device.
Philips North America
Patient support table floor plate may be incorrectly installed.
Philips North America
Patient support table floor plate may be incorrectly installed.
The product does not meet sterility assurance level.
Medical device components were marketed without FDA clearance
Human Care Hc Sweden Ab
Patient lift hanger bar may come loose, which could potentially pose risks to patients.
Medical device components were marketed without FDA clearance and without FDA approval