Recall Z-1861-2021— Skytron, Div. The KMW Group, Inc
Class II · Ongoing
Class II FDA medical device recall by Skytron, Div. The KMW Group, Inc, initiated 2021-05-11. FDA's recall record names no specific 510(k) clearance for this event. Product: Skyton Bracket Flatscreen, Revision 2 & 3-The FS32 is a single monitor mounting bracket intended for use with a 32 inch (maximum) flat screen monitor. Model: FS32. Reason: 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.
- Recalling firm
- Skytron, Div. The KMW Group, Inc
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2021-05-11
- Firm location
- Grand Rapids, MI, United States
Product description
Skyton Bracket Flatscreen, Revision 2 & 3-The FS32 is a single monitor mounting bracket intended for use with a 32 inch (maximum) flat screen monitor. Model: FS32
Reason for recall
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
Data sourced from openFDA. This site is unofficial and independent of the FDA.