Skyton Bracket Flatscreen — Class II medical device recall Z-1861-2021
Ongoing recall by Skytron, Div. The KMW Group, Inc, reported 2021-06-23, distributed nationwide. Failure of the FS32 Monitor Brackets from the mounting block could potentially loosen over time and eventually
| Recall number | Z-1861-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Skytron, Div. The KMW Group, Inc, Grand Rapids, MI, United States |
| Recall initiated | 2021-05-11 |
| Classified | 2021-06-15 |
| Reported by FDA | 2021-06-23 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, JP |
| Reason classes | device malfunction |
| 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 and 261 more |
| Model numbers | FS32 |
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 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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1861-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.