DELTA XTEND 2317-70-024Recalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10603295532460), received between Aug 19, 2022 and Dec 9, 2024 — classified as 6 malfunctions.

The most frequently reported specific device problem is “Device-Device Incompatibility” (5 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 16, 2026.

Most reported problems

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• MalfunctionDec 9, 2024Mechanical Jam; Mechanical Jam

  IT WAS REPORTED THAT TWO INSTRUMENTS IN THIS CASE MALFUNCTIONED: THE FIRST AUGMENT REAMER HANDLE HAD A BUTTON NEAR THE BACK END WHICH IS SPRING LOADED TO CAPTURE THE HUDSON ADAPTOR CONNECTION. THIS BUTTON WAS STICKING AND REQUIRED THE TECH TO TAP IT ON THE SIDE REPEATEDLY TO SPRING THE BOTTOM UP. THIS SHOULD NOT BE NECESSARY. THE SECOND CENTRAL SCREW, METAGLENE AUGMENTED METAGLENE REAMER HEAD BROKE WHILE REAMING THE GLENOID. THIS LEFT FRAGMENTS IN THE PATIENT WHICH REQUIRED THE SURGEON TO REMOVE.

  Patient problems: Insufficient Information

  MAUDE report 20885764 ↗
• MalfunctionMar 27, 2024Device-Device Incompatibility; Unintended Movement; Device-Device Incompatibility; Unintended Movement

  UPON RUNNING THE CSM REAMER, IT CAUSED THE DRILL TO SHAKE NOTICEABLY, AND REMAINED DOING SO AFTER RE-ASSEMBLY A NUMBER OF TIMES. THERE WAS A 5 MINUTE DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18987355 ↗
• MalfunctionJun 9, 2023Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED THAT THE REAMER LOCKED UP AND WOULDN'T SPIN. IT ALSO GOT STUCK ON THE HANDLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17098714 ↗
• MalfunctionFeb 21, 2023Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED THAT WHEN PUTTING TOGETHER THE FULL WEDGE AUGMENTED REAMER, THE CONSTRUCT WOULD NOT PROPERLY ENGAGE. THERE WAS A 15-20 MINUTES OF SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16409367 ↗
• MalfunctionAug 30, 2022Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED THAT THE CSM AUGMENT REAMER HAND PIECE TOLERANCE IS DEFECTIVE AND WILL NOT ACCEPT THE REAMER SHAFT BECAUSE IT DOESN¿T FIT. THIS INSTRUMENT HAS NEVER BEEN USED. THE REAMER SHAFT TOLERANCES WERE DOUBLE CHECKED WITH A DIFFERENT HANDLE AND THEY WERE CORRECT. NO SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15324422 ↗
• MalfunctionAug 19, 2022Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED THAT THE AUGMENT HANDLE REAMER WILL NOT TAKE AUGMENT REAMER HOUSING. AUGMENT REAMER HOUSING WILL SEAT INTO A DIFFERENT AUGMENT HANDLE REAMER OF THE SAME PART AND LOT NUMBER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15257989 ↗