MULTILOC
Received Apr 28, 2026 · Event occurred Apr 13, 2026
Report 8030965-2026-03912 · MDR key 25016884
Device
Product problems
- Break
Patient
NA · Unknown
- No Clinical Signs, Symptoms or Conditions
Narrative
Additional Manufacturer Narrative
PRODUCT COMPLAINT # (B)(4) THIS REPORT IS BEING SUBMITTED PURSUANT TO THE PROVISIONS OF 21 CFR, PART 803 (AND/OR PART 4, AS APPLICABLE). THIS REPORT MAY BE BASED ON INFORMATION WHICH HAS NOT BEEN INVESTIGATED OR VERIFIED PRIOR TO THE REQUIRED REPORTING DATE. THIS REPORT DOES NOT REFLECT A CONCLUSION BY DEPUY SYNTHES, OR ITS EMPLOYEES THAT THE REPORT CONSTITUTES AN ADMISSION THAT THE PRODUCT, DEPUY SYNTHES, OR ITS EMPLOYEES CAUSED OR CONTRIBUTED TO THE POTENTIAL EVENT DESCRIBED IN THIS REPORT. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL REPORT, A FOLLOW-UP REPORT WILL BE FILED AS APPROPRIATE.
Description of Event or Problem
IT WAS REPORTED THAT (B)(6) 2026, THE PATIENT UNDERWENT ORIF SURGERY FOR FRACTURE OF THE HUMERAL SHAFT FOR HUMERAL SHAFT. BEFORE THE SURGERY, UPON CHECKING THE EQUIPMENT, IT WAS FOUND THAT THE PRODUCT IN QUESTION WAS DAMAGED. THE PRODUCT IN QUESTION WAS NOT STERILIZED, AND ANOTHER INSTRUMENT WAS USED AS A SUBSTITUTE. THE SURGERY WAS COMPLETED SUCCESSFULLY WITH NO SURGICAL DELAY. NO FURTHER INFORMATION IS AVAILABLE.