FDA Device recall Z-2734-2016
2 over 2 Elevating Monitor Suspension - Omega Medical Imaging, LLC Elevating Monitor Suspension Systems
- FDA Device
- Class II
- terminated
- Published 2016-09-14
On 2016-09-14 the FDA classified a Class II recall of 2 over 2 Elevating Monitor Suspension - Omega Medical Imaging, LLC Elevating Monitor Suspension Systems by Omega Medical Imaging, citing elevating Monitor Suspension separated from the lifting column bracket.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2734-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-06-21 |
| Published | 2016-09-14 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Omega Medical Imaging |
| Distribution | AL, CO, GA, IL, IN, KY, LA, MN, MO, NC, NY, OH, PA, SD |
Product
2 over 2 Elevating Monitor Suspension - Omega Medical Imaging, LLC Elevating Monitor Suspension Systems.
Reason
Elevating Monitor Suspension separated from the lifting column bracket
Identifiers
| code_info | Model: Elevating Monitor Suuspension P/Ns: 1000-0085, 1000-0095 and (1000-0129 one unit produced does not use bracket 1040-0071 or 1040-0031). |
|---|
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-2734-2016%22
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