FDA Device recall Z-2868-2018
EasyDiagnost Eleva DRF, Release 5 (Stitching Patient Support) 706050
- FDA Device
- Class II
- terminated
- Published 2018-08-29
On 2018-08-29 the FDA classified a Class II recall of EasyDiagnost Eleva DRF, Release 5 (Stitching Patient Support) 706050 by Philips Medical Systems Dmc, citing the hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2868-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-06-27 |
| Published | 2018-08-29 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Philips Medical Systems Dmc |
| Distribution | US |
Product
EasyDiagnost Eleva DRF, Release 5 (Stitching Patient Support) 706050
Reason
The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
Identifiers
| code_info | Serial Numbers: SN17000027 SN16000011 SN16000014 SN16000036 SN16000015 SN15000050 476034/SN12000027 476338/SN12000026…Serial Numbers: SN17000027 SN16000011 SN16000014 SN16000036 SN16000015 SN15000050 476034/SN12000027 476338/SN12000026 SN17000022 SN15000029 SN16000017 SN16000009 SN13000078 SN16000048 SN16000004 SN13000029 SN14000068 511923/SN12000044 514827/SN12000098 514827/SN12000098 SN14000044 ***Updated 5/6/21*** SN15000055 |
|---|
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-2868-2018%22
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