Integra® Jarit® 277274TIRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10381780208525), received between Oct 16, 2025 and Oct 16, 2025 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (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. How this data works · Data updated Oct 13, 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.

• InjuryOct 16, 2025Break; Break

  A FACILITY REPORTED THAT THE RHOTON-TYPE BALL DISS 71/2 90D TT (277274TI) INSTRUMENT BROKE AT A 90-DEGREE ANGLE AT THE TIP AND WAS LEFT IN THE PATIENT. ACCORDING TO ADDITIONAL INFORMATION RECEIVED FROM THE STERILE PROCESSING SUPERVISOR, IT WAS NOTED THAT THE NEUROSURGERY RESIDENT AND THE OPERATING ROOM TEAM WHO WORKED ON THE CASE STATED THAT THE BROKEN PART WAS NOT RECOVERED, AND THE FLUOROSCOPY X-RAY THAT WAS PERFORMED DID NOT DETECT ANY BROKEN PIECES. IT WAS ALSO CONVEYED THAT THE PATIENT WAS UNDER GENERAL ANESTHESIA DURING THE PROCEDURE, AND THE OPERATING ROOM TEAM TRIED TO RETRIEVE THE BROKEN PIECE AFTER "COMMITTING A SIGNIFICANT AMOUNT OF TIME TRYING TO TAKE THE BROKEN PIECE OUT, " BUT IT WAS UNSUCCESSFUL. ACCORDING TO THE NEUROSURGERY RESIDENT, THE PIECE MIGHT HAVE BEEN SUCTIONED OUT WHEN HE WAS DISSECTING TO REMOVE IT, AND THE PATIENT WAS NOTIFIED OF THE INCIDENT." A DIFFERENT INSTRUMENT THAT WAS AVAILABLE WAS USED TO COMPLETE THE SURGERY. POSTOPERATIVELY, THE PATIENT HAD THE SURGERY ON (B)(6) 2025, WAS DISCHARGED ON (B)(6) 2025, AND HAD A RE-ADMISSION DUE TO A COMPLAINT OF NECK PAIN ON (B)(6) 2025 AND DISCHARGED ON (B)(6) 2025.

  Patient problems: Foreign Body In Patient

  MAUDE report 23318716 ↗