DELTA XTEND 2307-99-002Recalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10603295116622), received between Oct 23, 2018 and Apr 1, 2025 — classified as 7 malfunctions.

The most frequently reported specific device problem is “Device-Device Incompatibility” (4 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 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 1, 2025Device-Device Incompatibility; Material Deformation; Device-Device Incompatibility; Material Deformation

  IT WAS REPORTED THAT DURING A REVERSE SHOULDER PROCEDURE THE INTERNAL SCREW IN THE METAGELENE TRIAL CAME OUT. THE SURGEON AND SCRUB NURSE THOUGHT IT WAS BECAUSE THE T-HANDLE'S THREAD WAS BARE AND THEREFORE WASN¿T SCREWING BUT PUSHING ON THE TRIAL SCREW. NO DETERMINANT TO THE PATIENT. MINOR DELAY TO SURGERY DUE TO THE BACK UP KIT BEING OPENED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21740082 ↗
• MalfunctionJan 23, 2023Device-Device Incompatibility; Naturally Worn; Device-Device Incompatibility; Naturally Worn

  IT WAS REPORTED THAT THE EXTRACTION T-HANDLE GOT CROSS THREADED INSIDE THE HUMERAL SPACER TRIAL +9 AND COULD NOT BE DISASSEMBLED AFTER CASE. THESE ITEMS ARE FROM OFFICE SET. NO SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16225380 ↗
• MalfunctionOct 4, 2022Device-Device Incompatibility; Device-Device Incompatibility

  TRIAL HAS A LARGE FRACTURE, ALSO NOTED IS THAT THE THREADED INSERT WITHIN THE TRIAL HAS BECOME DISLODGED FROM THE TRIAL BODY. EXTRACTION T HANDLE HAS SEIZED ONTO THE DISLODGED TRIAL THREADED INSERT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15536679 ↗
• MalfunctionOct 7, 2021Break; Break

  IT WAS REPORTED THAT ONE OF THE TEETH BROKE OFF DURING THE PROCEDURE. NO PATIENT CONSEQUENCE MENTIONED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12591296 ↗
• MalfunctionAug 10, 2021Material Deformation; Material Deformation

  IT WAS REPORTED THAT THE METAGLENE EXTRACTOR WAS BENT AND WOULD NOT ENGAGE. NOTHING LEFT IN PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12300377 ↗
• MalfunctionJun 2, 2021Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED THAT THE T-HANDLE BECAME LOCKED ONTO THE METAGLENE AND WOULD NOT DISENGAGE FROM IT. NO SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11925135 ↗
• MalfunctionOct 23, 2018Break; Break

  IT WAS REPORTED THAT THE INSTRUMENT BROKE DURING NORMAL USE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7995567 ↗