DELTA XTEND
Received May 27, 2026 · Event occurred May 6, 2026
Report 1818910-2026-09272 · MDR key 25303033
Device
Generic name
Delta Xtend Implants : Screws
Manufacturer
Depuy Orthopaedics Inc UsCatalog number
130770018
Lot number
5665850
Product problems
- Adverse Event Without Identified Device or Use Problem
Patient
69 YR · Female
- Unspecified Infection
Narrative
Description of Event or Problem
IT WAS REPORTED THAT PATIENT REVISED DUE TO INFECTION. EVERYTHING TAKEN OUT. DOI: (B)(6) 2024 DOR: (B)(6) 2026 AFFECTED SIDE: LEFT.
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 MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE.