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
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📍Recalling firmSkytron, Div. The KMW Group, Inc5085 Corporate Exchange Blvd SE · Grand Rapids, MI 49512-5515
✎ GovInfoNow plain-language explainer
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. Read more at govinfonow.com/recall/62576-skyton-bracket-flatscreen-revision-2-3-fs32-monitor-bracket-recall.
“Skyton Bracket Flatscreen Revision 2 & 3 FS32 Monitor Bracket Recall: Risk of Injury.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/62576-skyton-bracket-flatscreen-revision-2-3-fs32-monitor-bracket-recall. Based on FDA recall #Z-1861-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1861-2021%22&limit=1).
The Food and Drug Administration announced on May 11, 2021, that Skytron is recalling FS32 monitor brackets due to a potential hazard where the bracket could detach from its baseplate. This failure may cause the display interface to dismount, posing an injury risk to patients or staff.
Serial Numbers: 1504-314-00-1-0002 through 2006-314-00-1-0185 and 2011-314-00-2-0002 through 2103-314-00-2-0170
The hazard
The FS32 Monitor Brackets may loosen over time and eventually detach from the baseplate. This can result in the display interface dismounting from its attachment point, causing injury to patients or staff.
Context
GovInfoNow's records show Skytron has issued five other recalls since April 18, 2019. Other recent recalls of similar products include Siemens ARTIS icono Ceiling Monitor Recall (June 8, 2026), Philips Azurion System Recall (March 31, 2026), and Canon Alphenix X-ray Systems Recall (August 4, 2026).
How to tell if you have this one
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.
Brand
Skytron
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check for Recalled Serial Numbers
Look for serial numbers starting with 1504-314-00-1-0002 up to 2011-314-00-2-0170 on the bracket.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “Worldwide distribution - US Nationwide and the countries of Australia, Japan.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 43 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-1861-2021 (May 11, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1861-2021 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.