FDA Device recall Z-2621-2017
Omega Medical Imaging - 2 over 2 Elevating Monitor Suspension pillar/column accessory Device accessory that elevates monitor for healthcare…
- FDA Device
- Class II
- terminated
- Published 2017-06-28
On 2017-06-28 the FDA classified a Class II recall of Omega Medical Imaging - 2 over 2 Elevating Monitor Suspension pillar/column accessory Device accessory that elevates monitor for healthcare… by Omega Medical Imaging, citing elevating Monitor Suspension column dropping and will not rise back up.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2621-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-03-23 |
| Published | 2017-06-28 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Omega Medical Imaging |
| Distribution | IN, MT, OH, PA |
Product
Omega Medical Imaging - 2 over 2 Elevating Monitor Suspension pillar/column accessory Device accessory that elevates monitor for healthcare professionals.
Reason
Elevating Monitor Suspension column dropping and will not rise back up.
Identifiers
| code_info | SKF Telescopic Pillar P/N ending in -003 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2621-2017%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.