Thompson 10045511Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00841536100143), received between Apr 7, 2026 and Apr 7, 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 16, 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.

• InjuryApr 7, 2026Adverse Event Without Identified Device or Use Problem

  2025-FEB-14 MPXR 1272358 (REP, HCP, FOR): INFORMATION WAS RECEIVED FROM HEALTHCARE PROVIDER (HCP) VIA A MANUFACTURER REPRESENTATIVE REGARDING A PATIENT IMPLANTED WITH CAGE HAVING SPINAL THERAPY FOR INTESTINAL INJURY, IT WAS REPORTED THAT A PATIENT WHO UNDERWENT SURGERY (FM/T3) YESTERDAY WAS SUSPECTED OF HAVING INTESTINAL DAMAGE. DUE TO THE SUSPICION OF INTESTINAL DAMAGE, THE SURGICAL DOCTOR PERFORMED AN OPERATION TO RESECTION THE BOWEL AND REPLACED IT WITH ARTIFICIAL ANUS. IT WAS SPECULATED BY THE ORTHOPEDIC DOCTOR THAT A RETRACTOR OR SOMETHING SIMILAR MIGHT HAVE INJURED THE INTESTINE DURING THE INITIAL T3 OPERATION. NO SYMPTOMS WERE PRESENT WHEN THE INITIAL SURGERY CONCLUDED YESTERDAY. IT IS ANTICIPATED THAT SYMPTOMS MIGHT HAVE APPEARED FROM POST OPERATION (INITIAL OPERATION) TO THIS NEXT DAY MORNING. THE SURGICAL OPERATION WAS PERFORMED WITHOUT THE REMOVAL OF THE T3. THERE WERE NO FURTHER COMPLICATIONS REPORTED REGARDING THE EVENT. 2025-FEB-19 ARED (REP): ADDITIONAL INFORMATION RECEIVED THAT IT IS NOT CLEAR WHETHER THE CAUSE WAS THE RETRACTION. IT IS UNKNOWN WHICH INSTRUMENT ACTUALLY CAUSED THE INTESTINAL DAMAGE. THERE ARE NO DEFECTS IN THE IMPLANTS USED. THE REASON FOR THE REMOV

  Patient problems: Bowel Perforation

  MAUDE report 24802576 ↗