FDA Device recall Z-1861-2021
Skyton Bracket Flatscreen, Revision 2 & 3-The FS32 is a single monitor mounting bracket intended for use with a 32 inch (maximum) flat scre…
- FDA Device
- Class II
- ongoing
- Published 2021-06-23
On 2021-06-23 the FDA classified a Class II recall of Skyton Bracket Flatscreen, Revision 2 & 3-The FS32 is a single monitor mounting bracket intended for use with a 32 inch (maximum) flat scre… by Skytron Div The Kmw Group, citing 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 dismounti….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1861-2021 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2021-05-11 |
| Published | 2021-06-23 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Skytron Div The Kmw Group |
| Distribution | US |
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
Identifiers
| code_info | Serial Numbers: 1504-314-00-1-0002 up to 2006-314-00-1-0185 ***UPDATED 12/10/21*** Recall expanded to include Rev 3.…Serial Numbers: 1504-314-00-1-0002 up to 2006-314-00-1-0185 ***UPDATED 12/10/21*** Recall expanded to include Rev 3. Complete list of recalled Serial Numbers: 1504-314-00-1-0002 1504-314-00-1-0003 1504-314-00-1-0004 1508-314-00-1-0005 1508-314-00-1-0006 1508-314-00-1-0007 1508-314-00-1-0008 1509-314-00-1-0009 1509-314-00-1-0010 1509-314-00-1-0011 1509-314-00-1-0012 1510-314-00-1-0013 1510-314-00-1-0014 1601-314-00-1-0016 1601-314-00-1-0017 1610-314-00-1-0018 1610-314-00-1-0019 1610-314-00-1-0020 1610-314-00-1-0021 1610-314-00-1-0022 1610-314-00-1-0023 1610-314-00-1-0024 1610-314-00-1-0025 1610-314-00-1-0026 1610-314-00-1-0027 1610-314-00-1-0028 1610-314-00-1-0029 1610-314-00-1-0030 1610-314-00-1-0031 1610-314-00-1-0032 1802-314-00-1-0033 1802-314-00-1-0034 1802-314-00-1-0035 1802-314-00-1-0036 1802-314-00-1-0037 1802-314-00-1-0038 1802-314-00-1-0039 1802-314-00-1-0040 1802-314-00-1-0041 1802-314-00-1-0042 1803-314-00-1-0043 1803-314-00-1-0044 1803-314-00-1-0045 1803-314-00-1-0046 18 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1861-2021%22
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