EasyDiagnost Eleva 9890-010-03632Recalls & reported problems
Philips Medical Systems DMC GmbH · Table, Radiographic, Tilting · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00884838074255), received between Jul 7, 2025 and Jun 16, 2026 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Recalls naming this device
- Sep 21, 2023Open, Classified
Potential for units suspended on the ceiling to fail and fall.
Z-0279-2024 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported problems
Device problems
- Detachment of Device or Device Component1
- Unintended Collision1
Patient problems
- Bone Fracture(s)1
- Laceration(s)1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 16, 2026Detachment of Device or Device Component
IT WAS REPORTED THAT THE FOOTREST WAS NOT LOCKING TO TABLETOP FOR USE. THE DEVICE WAS OUTSIDE CLINICAL USE AND THERE WAS NO PATIENT OR USER HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25514333 ↗InjuryJul 7, 2025Unintended Collision; Unintended Collision
IT WAS REPORTED THAT THE FIELD SERVICE ENGINEER (FSE) INJURED AT CUSTOMER SITE, ON EASY DIAGNOSTIC ELEVA SYSTEM SERVICE. THE DEVICE WAS OUTSIDE OF CLINICAL USE.
Patient problems: Bone Fracture(s); Laceration(s)
MAUDE report 22409920 ↗
Other Table, radiographic, tilting devices
- Sonesta 6210Sonesta Medical AB · Table, Radiographic, Tilting1 recall1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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