DELTA XTEND 2307-60-038Recalls & reported problems

Summary

The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 10603295115960), received between Aug 31, 2017 and Jan 8, 2025 — classified as 9 malfunctions.

The most frequently reported specific device problem is “Break” (7 reports).

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 18, 2026.

Most reported problems

Recent adverse event reports

The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.

• MalfunctionJan 8, 2025Break; Illegible Information; Break; Illegible Information

  IT WAS REPORTED THAT PLASTIC PARTICLES COME LOOSE, AND THEY ARE SLUGGISH TO PUT ON THE ORIGINAL METAGLENPLATE DURING TESTING. ALL SURGERIES HAVE ABOUT A 5 MINUTE DELAY BECAUSE OF THIS. THE LOT NUMBER WAS TOO SMALL TO BE READ.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21105210 ↗
• MalfunctionJan 8, 2025Break; Device-Device Incompatibility; Illegible Information; Break; Device-Device Incompatibility; Illegible Information

  IT WAS REPORTED THAT PLASTIC PARTICLES COME LOOSE AND THEY ARE SLUGGISH TO PUT ON THE ORIGINAL METAGLENPLATE DURING TESTINGCAN NOT READ LOT NO. IT IS TOO SMALLALL SURGERIES HAVE ABOUT 5 MIN DELAY BECAUSE OF THIS. THE EVENT DAY UNKNOWN, EVENT MONTH DECEMBER 2024.

  Patient problems: Insufficient Information

  MAUDE report 21101748 ↗
• MalfunctionJan 6, 2025Break; Break

  IT WAS REPORTED THAT THE ECC GLENOSPHERE TRIAL DISC 38 MM 230760038 IS QUITE FRAYED WITH SMALL BITS OF PLASTIC PEELING OFF. THERE WAS NO SURGICAL DELAY. THERE WERE NO PATIENT CONSEQUENCES.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21078891 ↗
• MalfunctionNov 2, 2023Break; Scratched Material; Break; Scratched Material

  TRIAL GLENOSPHERES ARE SCRATCHED ON THE BACKSIDE, SMALL PLASTIC FRAGMENTS WERE LOOSENING FROM THE TRIAL IMPLANT DURING INSERTION/ REMOVAL. PROCEDURE SUCCESSFULLY COMPLETED WITH NO SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18056038 ↗
• MalfunctionApr 8, 2020Mechanical Jam; Mechanical Jam

  IT WAS REPORTED THAT WHEN TRYING TO "USED" GLENOSPHERE TRIAL, SCREW PUSHED THRU PLASTIC AND BECAME UNUSABLE. ALL PIECES RETRIEVED. NO SURGICAL DELAY.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9934119 ↗
• MalfunctionNov 22, 2019Break; Physical Resistance/Sticking; Break; Physical Resistance/Sticking

  IT WAS REPORTED THAT WHEN ATTEMPTING TO ATTACHED THE HANDLE TO 38 ECC GLENOSPHERE TRIAL, THE METAL CONNECTION PUSHED THROUGH PLASTIC AND BECAME UNUSABLE. NO SURGICAL DELAY.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9362400 ↗
• MalfunctionJan 17, 2019Break; Break

  IT WAS REPORTED THAT THE TRIAL EPIPHYSIS SIZE 38MM ECCENTRIC WAS BROKEN PRIOR TO SURGERY.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8257614 ↗
• MalfunctionJul 16, 2018Connection Problem; Naturally Worn; Connection Problem; Naturally Worn

  IT WAS REPORTED THAT DURING TRIALING OF THE 38 ECC GLENOSPHERE, THE METAL THREADED PORTION OF THE TRIAL BECAME LOOSE AND SEPARATED FROM THE PLASTIC, MAKING IT UNUSABLE. PLASTIC HAS BEEN STRIPPED WHERE METAL PORTION THREADS INTO IT.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7691274 ↗
• MalfunctionAug 31, 2017Break; Break

  IT WAS REPORTED THAT BOTH INSTRUMENTS WERE BROKEN DURING SURGERY. THE GLENOSPHERE ECC TRIAL LOST THE MIDDLE RING TO WHICH YOU SCREW ONTO THE T-HANDLE.

  Patient problems: No Information

  MAUDE report 6836113 ↗