DELTA XTEND 1307-62-042Recalls & reported problems

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 10603295502449), received between Oct 22, 2020 and Dec 28, 2023 — classified as 6 injuries, 2 malfunctions.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (2 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 8 most recent of 8 reports, in the reporter's own words as published by the FDA.

• InjuryDec 28, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated

  PATIENT WAS REVISED DUE TO LOOSENING OF GLENOSPHERE. GLENOSPHERE WAS OFF THE METAGLENE/BASEPLATE, AND WAS REVISED TO A NEW. DOI: (B)(6) 2023. DOR: (B)(6) 2023. AFFECTED SIDE: RIGHT SHOULDER.

  Patient problems: Insufficient Information

  MAUDE report 18413140 ↗
• InjuryMar 9, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  REVISION COMPLETED DUE TO INFECTION. SURGEON DECIDED TO REMOVE THE CONSTRUCT AND IMPLANT AN ANTIBIOTIC SPACER. DOI: (B)(6) 2022. DOR: (B)(6) 2023. AFFECTED SIDE: RIGHT SHOULDER.

  Patient problems: Unspecified Infection

  MAUDE report 16516962 ↗
• InjuryNov 14, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated

  REVISION COMPLETED DUE TO DISLOCATION. THERE WAS NO SURGICAL DELAY. DOI: UNKNOWN; DOR: (B)(6) 2022; AFFECTED SIDE: RIGHT SHOULDER.

  Patient problems: Joint Dislocation

  MAUDE report 15793903 ↗
• MalfunctionOct 12, 2022Fracture; Fracture

  IT WAS REPORTED THAT THE GLENOSPHERE THREAD BROKEN 2X.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15587287 ↗
• InjuryJun 2, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT WAS CONVERTED FROM A REVERSE TSA TO A HEMI WITH CTA HEAD DUE TO SHOULDER PAIN. DOI: (B)(6) 2020, DOR: (B)(6) 2022, AFFECTED SIDE: RIGHT SHOULDER.

  Patient problems: Pain

  MAUDE report 14575592 ↗
• InjuryMay 19, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED DUE TO INFECTED TOTAL SHOULDER. THE SURGEON DETERMINED IT BEST TO REMOVE ALL IMPLANTS AND PUT IN A COMPETITOR SPACER UNTIL THE INFECTION CLEARED. NO FURTHER PATIENT INFORMATION IS AVAILABLE AT THIS TIME. DOI: (B)(6) 2021; DOR: (B)(6) 2022; AFFECTED SIDE: RIGHT SHOULDER.

  Patient problems: Unspecified Infection

  MAUDE report 14433902 ↗
• InjuryApr 26, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED FROM A REVERSE TO A HEMI WITH CTA HEAD DUE TO PAIN. GLENOSPHERE LOOSENING WAS ALSO REPORTED AT THE BONE TO IMPLANT INTERFACE. DOI: (B)(6) 2020; DOR: (B)(6) 2022; AFFECTED SIDE : RIGHT SHOULDER.

  Patient problems: Pain

  MAUDE report 14205688 ↗
• MalfunctionOct 22, 2020Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT NEITHER OF THE GLENOSPHERES WOULD THREAD INTO THE METAGLENE. THE THREADS APPEARED TO GET DAMAGED SOMEHOW. THE SURGEON FELT LIKE SOMETHING MAY HAVE BEEN WRONG WITH THE METAGLENE. BUT THE THIRD ONE WE TRIED FINALLY THREADED IN. A SURGICAL DELAY OF 10 MINUTES. DOE: (B)(6) 2020 LEFT SHOULDER.

  Patient problems: No Code Available

  MAUDE report 10720733 ↗