FDA Device recall Z-0156-2024
Omega Medical Imaging Elevating Monitor Suspension, Part Number 1000-0085
- FDA Device
- Class II
- ongoing
- Published 2023-11-01
On 2023-11-01 the FDA classified a Class II recall of Omega Medical Imaging Elevating Monitor Suspension, Part Number 1000-0085 by Omega Medical Imaging, citing an actuator separated from the pivot mechanism on a lower monitor boom system column and became detached and was restrained by the installed safety cable at one location.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0156-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-02-28 |
| Published | 2023-11-01 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Omega Medical Imaging |
| Distribution | US |
Product
Omega Medical Imaging Elevating Monitor Suspension, Part Number 1000-0085
Reason
An actuator separated from the pivot mechanism on a lower monitor boom system column and became detached and was restrained by the installed safety cable at one location.
Identifiers
| code_info | all units manufactured between 10-22-2012 and 07-09-2019 |
|---|
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-0156-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.