Recall of Skyton Bracket Flatscreen Revision 2 & 3 FS32 monitor mounting brackets due to risk of detachment causing injury to patients or staff. Serial numbers listed in updated notice.
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
Skytron's FS32 monitor mounting brackets (Revisions 2 and 3) are being recalled because they can loosen over time and detach from the baseplate, potentially causing injury to patients or staff. This risk occurs when the bracket fails to stay securely attached to the monitor.
The bracket can loosen over time and eventually detach from the baseplate, causing the monitor to dismount from its attachment point. This could lead to injury to patients or staff if the monitor falls or moves unexpectedly.
Healthcare facilities using the recalled brackets for mounting 32-inch flat screens are most at risk. Patients and staff could be injured if the bracket detaches during use.
Check for the model number FS32 and serial numbers starting with 1504-314-00-1-0002 up to 2011-314-00-2-0170. The brackets are intended for use with 32-inch flat screen monitors.
Look for serial numbers starting with 1504-314-00-1-0002 up to 2011-314-00-2-0170 on the bracket.
Skytron's FS32 monitor mounting brackets (Revisions 2 and 3) are recalled because they can loosen over time and detach from the baseplate, potentially causing injury to patients or staff.
Check for the model number FS32 and serial numbers starting with 1504-314-00-1-0002 up to 2011-314-00-2-0170 on the bracket.
The recall does not specify a remedy, so contact Skytron directly for guidance on next steps.
We’ve drafted a message you can send Skytron to request your refund or repair — edit it as you like.
Subject: Recall Z-1861-2021 — Skytron Skytron Hello, I own a Skytron that is covered by recall Z-1861-2021 from Skytron. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
