Del Medical, Inc. EV800Recalls & reported problems
Del Medical, Inc. · The EV800 elevating table is designed for general purpose radiography and features a four-way floating table top with longitudinal and transverse travel. It uses electromechanical locks to maintain the desired position. It has a motor-driven telescopic base that can raise and lower the table top. It has a patient weight limit of 800 lbs. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00858340006028), received between Apr 18, 2026 and Apr 23, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (2 reports).
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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Device Dislodged or Dislocated2
- Unintended Movement1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 23, 2026Device Dislodged or Dislocated
ON (B)(6) 2026, THE CUSTOMER CONTACTED TS TO REPORT THAT THE EV 800 TABLETOP (SERIAL NUMBER (B)(6)) TILTED WHILE A PATIENT WAS ON IT. THE CUSTOMER CONFIRMED THAT NO INJURIES OCCURRED AS A RESULT OF THE INCIDENT. PICTURES FROM THE CUSTOMER SHOWED THE SPROCKET ADJUST WORN AND METAL SHAVINGS UNDERNEATH THE TABLETOP, IN A CAVITY NOT ACCESSIBLE TO THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24972127 ↗MalfunctionApr 18, 2026Device Dislodged or Dislocated; Unintended Movement
ON (B)(6) 2026, THE CUSTOMER CONTACTED TECHNICAL SERVICES (TS) TO REPORT THAT THE EV 800 TABLETOP (SERIAL NUMBER (B)(6)) DROPPED A FEW INCHES WHILE A PATIENT WAS ON IT. THE CUSTOMER CONFIRMED THAT NO INJURIES OCCURRED AS A RESULT OF THE INCIDENT. PICTURES FROM THE CUSTOMER SHOWED THE TABLETOP SECTION TILTED AND METAL SHAVINGS UNDERNEATH THE TABLETOP, IN A CAVITY NOT ACCESSIBLE TO THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24919880 ↗
Other Table, Radiographic, Non-Tilting, Powered devices
- Del Medical Inc. EV650Del Medical, Inc. · Table, Radiographic, Non-Tilting, Powered1 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
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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