NeuViz 64 Multi-slice CT Scanner System NeuViz 64 InRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 06970167440022), received between Oct 29, 2019 and Oct 29, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 29, 2019Device Dislodged or Dislocated; Device Fell; Device Fell

  THE GANTRY MYLAR OF NEUVIZ 64IN CT SCANNER DISLODGED AND CONTACTED A PATIENT. PATIENT PRESENTED MODERATED LACERATIONS IN THE RIGHT FOOT. THE DOCTOR MADE X-RAYS TO THE PATIENT'S FOOT AND DID SKIN TREATMENT.

  Patient problems: Laceration(s); Skin Tears

  MAUDE report 9248671 ↗