Del Medical Inc. EV650Recalls & reported problems
Del Medical, Inc. · The EV650 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 650 lbs. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00858340006011), received between May 27, 2021 and May 27, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (1 report).
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.
Most reported problems
Device problems
- Improper or Incorrect Procedure or Method1
- Labelling, Instructions for Use or Training Problem1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 27, 2021Labelling, Instructions for Use or Training Problem; Improper or Incorrect Procedure or Method
DURING A SERVICE CALL, THE MANUFACTURE'S TECHNICAL SUPPORT REPRESENTATIVE WAS PROVIDING INSTRUCTIONS TO THE THIRD PARTY SERVICE ENGINEER TO SUPPORT DIAGNOSING A PERFORMANCE ISSUE. WHILE THE MANUFACTURERS TECHNICAL SUPPORT REPRESENTATIVE BELIEVED HE WAS CLEARLY COMMUNICATING THAT HE WAS PREVIEWING THE INSTRUCTIONS,THE THIRD -PARTY ENGINEER BEGAN TO PERFORM THE OPERATIONS BEFORE RECEIVING THE COMPLETE SAFETY PRECAUTIONS INSTRUCTIONS. THE MANUFACTURER'S REPRESENTATIVE WAS VERBALLY WALKING THE THIRD-PARTY ENGINEER THROUGH SECTION 5.4 OF THE EV650 SERVICE MANUAL. THIS SECTION CONTAINS A WARNING IMMEDIATELY PRECEDING THE STEP WHERE THE INCIDENT OCCURRED THAT READS "PROCEED WITH CAUTION. THE FOLLOWING STEPS CARRY RISK OF INJURY OR EQUIPMENT DAMAGE. WHEN YOU MAKE THE FOLLOWING CONNECTION THE TABLE WILL BEGIN TO MOVE IMMEDIATELY. THE TABLE WILL STOP ONLY WHEN YOU DISCONNECT THE OVERRIDE CABLE. THE LIMI SWITCHES WILL STOP THE TABLE. TO AVOID DAMAGES STOP THE TABLE AS SOON AS IT IS BACK WITHIN LIMITS RANGE".
Patient problems: Insufficient Information
MAUDE report 11897721 ↗
Other Table, Radiographic, Non-Tilting, Powered devices
- Del Medical, Inc. EV800Del Medical, Inc. · Table, Radiographic, Non-Tilting, Powered2 reports
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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