EXPEDIUM VERSE 199721525Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10705034442488), received between Oct 13, 2017 and Oct 13, 2017 — classified as 4 injuries.

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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjuryOct 13, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  AFTER SURGERY THE PATIENT WOKE UP WITH VERY LITTLE FEELING IN THEIR LEGS. POST-OP CT WAS DONE AND THE SURGEON IDENTIFIED FOUR SCREWS THAT HAD BEEN PLACED MEDIAL. (LEFT T3,T4,T6 AND RIGHT T6) REPLACEMENT. THE PATIENT WAS RETURNED TO THE OR AND FOUR SCREWS WERE REMOVED AND THE RODS AND CORRECTION KEYS WERE RE-IMPLANTED.

  Patient problems: Injury; Paraplegia; Spinal Column Injury

  MAUDE report 6949175 ↗
• InjuryOct 13, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  AFTER SURGERY THE PATIENT WOKE UP WITH VERY LITTLE FEELING IN THEIR LEGS. POST-OP CT WAS DONE AND THE SURGEON IDENTIFIED FOUR SCREWS THAT HAD BEEN PLACED MEDIAL. (LEFT T3,T4,T6 AND RIGHT T6) REPLACEMENT. THE PATIENT WAS RETURNED TO THE OR AND FOUR SCREWS WERE REMOVED AND THE RODS AND CORRECTION KEYS WERE RE-IMPLANTED.

  Patient problems: Injury; Paraplegia; Spinal Column Injury

  MAUDE report 6949168 ↗
• InjuryOct 13, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  AFTER SURGERY THE PATIENT WOKE UP WITH VERY LITTLE FEELING IN THEIR LEGS. POST-OP CT WAS DONE AND THE SURGEON IDENTIFIED FOUR SCREWS THAT HAD BEEN PLACED MEDIAL. (LEFT T3,T4,T6 AND RIGHT T6) REPLACEMENT. THE PATIENT WAS RETURNED TO THE OR AND FOUR SCREWS WERE REMOVED AND THE RODS AND CORRECTION KEYS WERE RE-IMPLANTED.

  Patient problems: Injury; Paraplegia; Spinal Column Injury

  MAUDE report 6949095 ↗
• InjuryOct 13, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  AFTER SURGERY THE PATIENT WOKE UP WITH VERY LITTLE FEELING IN THEIR LEGS. POST-OP CT WAS DONE AND THE SURGEON IDENTIFIED FOUR SCREWS THAT HAD BEEN PLACED MEDIAL. (LEFT T3,T4,T6 AND RIGHT T6) REPLACEMENT. THE PATIENT WAS RETURNED TO THE OR AND FOUR SCREWS WERE REMOVED AND THE RODS AND CORRECTION KEYS WERE RE-IMPLANTED.

  Patient problems: Injury; Paraplegia; Spinal Column Injury

  MAUDE report 6948941 ↗