RECLAIM
Received Jun 22, 2026 · Event occurred May 28, 2026
Report 1818910-2026-10597 · MDR key 25578294
Device
Generic name
Hip Instrument - Reamer
Manufacturer
Depuy Ireland - 3015516266Catalog number
440000032
Lot number
SO2059870
Product problems
- Device-Device Incompatibility
- Material Deformation
Patient
Female
- No Clinical Signs, Symptoms or Conditions
Narrative
Description of Event or Problem
IT WAS REPORTED THAT THE REAMER EXTENSION SHAFT WOULD NOT CONNECT TO THE BLACK HANDLE OR THE POWER HUDSON ATTACHMENT. SURGEON GOT REAMER STUCK AND MAY HAVE BENT IT TRYING TO REMOVE FROM PATIENT.
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.