Hana Orthopedic Surgery Table (int'l) 6875IRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00842430107474), received between Aug 15, 2019 and Aug 15, 2019 — 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

Recent adverse event reports

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

• InjuryAug 15, 2019Improper or Incorrect Procedure or Method; Insufficient Device Problem Information; Improper or Incorrect Procedure or Method; Insufficient Device Problem Information

  IT WAS REPORTED PATIENT FELL OFF THE SURGERY TABLE DURING SURGERY. PATIENT BUMPED HEAD WITH NO APPARENT INJURY. SAFETY STRAP WAS NOT APPLIED TO THE PATIENT WHEN SHE FELL OFF THE TABLE. TOE WAS BROKEN IN FALL. TOTAL HIP ARTHROPLASTY AS COMPLETED SUCCESSFULLY AT A LATER DATE.

  Patient problems: Bone Fracture(s); Fall

  MAUDE report 8896488 ↗