EasyDiagnost Eleva DRF — Class II medical device recall Z-2867-2018
Terminated recall by Philips Medical Systems Gmbh, DMC, reported 2018-08-29, distributed nationwide. The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or s
| Recall number | Z-2867-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Medical Systems Gmbh, DMC, Hamburg, Germany |
| Recall initiated | 2018-06-27 |
| Classified | 2018-08-17 |
| Reported by FDA | 2018-08-29 |
| Terminated | 2024-04-30 |
| Distributed | Nationwide (US) |
| Serial numbers | 470350/SN10000103, 475222/SN11000013, 482735/SN11000053, 484559/SN11000063, 486215/SN11000104, 499144/SN12000035, 502428/SN12000048, 505693/SN12000054, 77124552 |
Product
EasyDiagnost Eleva DRF (Stitching Patient Support) 706032
Reason for recall
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.
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-2867-2018. 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.