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Skytron, Div. The KMW Group Recalls
9 recalls on record · January 20, 2016 to July 6, 2022 · Medical Devices
Recalls by year
16
19
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22
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
July 6, 2022Medical DevicesFDA
Skytron, Div. The KMW Group, Inc recalls Product Name: GCX Channel Mounting Accessory Model/Catalog Number: H8-300-40-A
Hazard: Under certain circumstances, the mounting screws may loosen or pull out from the attachment point on the Ergon 3 boom when the GCX Channel Mounting Accessory was used with the VST clamp as a monitor mount on the boom.
June 23, 2021Medical DevicesFDA
Skytron, Div. The KMW Group, Inc recalls Skyton Bracket Flatscreen, Revision 2 & 3-The FS32 is a single monitor mounting bracket intended for use with a 32 inch
Hazard: Failure of the FS32 Monitor Brackets from the mounting block could potentially loosen over time and eventually detach from the baseplate, result in the display interface dismounting from its attachment point, causing injury to patients or staff
October 21, 2020Medical DevicesFDA
Skytron, Div. The KMW Group, Inc recalls SkyVision SDS System - Video Integration Model: GC-SDS-BSCB-200 - Product Usage: is a high quality, self-contained vide
Hazard: Intermittent failure of a signal being sent to a monitor from the touch panel display causing the displaying monitor to go Blank and the touch panel to display a Blank image when reviewing the target display. If this issue were to happen during a case, cause increase risk to patient due to hospital losing the visual image.
October 14, 2020Medical DevicesFDA
Skytron, Div. The KMW Group, Inc recalls VGDF-SKY (R4-010-06) VGA TO FIBER CONVERTER-Single Format Faceplate, a component of the SkyVision Linx 300 Integration C
Hazard: VGDF (VGA) Faceplate failure results in failure of video signal for SkyVision Linx 300, a secondary display. Video would continue on the primary source device display
April 1, 2020Medical DevicesFDA
Skytron, Div. The KMW Group, Inc recalls Skytron Ergon 3 Series Skyboom Monitor Bracket-Flatscreen Bracket, single monitor mount, 27" max. screen size Part n
Hazard: Potential for the weld to fail at the pivot point of the monitor bracket. This weld failure could cause the display interface and bracket to fall from its mounted location, resulting in injury.
June 19, 2019Medical DevicesFDA
Skytron, Div. The KMW Group, Inc recalls Skytron Integrity 270 Steam Sterilizer and Skytron Integrity 270VP Steam Product Usage: The SKYTRON Integrity 270 St
Hazard: Weld attaching the air heater assembly to the main sterilizer unit has shown signs of fatigue/failure
June 8, 2016Medical DevicesFDA
Skytron, Div. The KMW Group, Inc recalls Ergon III Series Skyboom Monitor Bracket. Part # 3FCM1 Flatscreen Bracket, single monitor mount, 27inch max. screen siz
Hazard: Potential for the weld to fail at the pivot point of the monitor bracket. This weld failure could cause the display interface and bracket to fall from its mounted location, resulting in injury.
June 8, 2016Medical DevicesFDA
Skytron, Div. The KMW Group, Inc recalls EZ Slide Battery/line powered hydraulic table with removable leg section and 21 top slide General Purpose Surgical Ta
Hazard: The potential exists within the identified tables that incorrectly manufactured parts have been used in assembly. If a table is found to have these incorrectly manufactured parts, it is possible for the tables elevation column slide cap to become detached from the elevation column and could result in the loss of control of the table top and injury to the patient or staff.
January 20, 2016Medical DevicesFDA
Skytron, Div. The KMW Group, Inc recalls Ergon 2 Articulating Equipment Boom Monitor Brackets mounting point for display interfaces utilized in clinical appli
Hazard: The hardware that holds the VESA plate and the display interface / monitor to the bracket may fail causing the display interface to fall from the bracket. Over time and with use the threaded rod hardware material can weaken and detach from the bracket. A display interface falling from its mounting location may result in injury to the patient or provider.