TABLE, HANA, 110 V, REFURBISHED 6875RRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00842430101656), received between Mar 11, 2026 and Mar 11, 2026 — classified as 1 injury.

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.

• InjuryMar 11, 2026Adverse Event Without Identified Device or Use Problem

  AN ELDERLY MAN WITH HIP AND RIB FRACTURES UNDERWENT HIP NAILING ON A HANA TABLE UNDER SPINAL ANESTHESIA AND LATER DEVELOPED COMPLETE LOWER EXTREMITY PARALYSIS. IMAGING REVEALED AN L1 FRACTURE WITH SUBLUXATION AND CORD COMPRESSION, REQUIRING EMERGENCY DECOMPRESSION AND FUSION, WITHOUT NEUROLOGIC RECOVERY. IT REMAINS UNCLEAR WHETHER THE SPINAL INJURY WAS PRE EXISTING OR DISPLACED DURING SURGERY, WITH HINDSIGHT SUGGESTING UNDERLYING SPINAL ANKYLOSIS (DISH) AND THAT ADDITIONAL SPINAL IMAGING OR ALTERNATIVE POSITIONING MAY HAVE REDUCED RISK.

  Patient problems: Bone Fracture(s); Vertebral Fracture

  MAUDE report 24573106 ↗