DELTA XTEND 1307-66-142Recalls & reported problems

Summary

The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 10603295502623), received between Mar 13, 2020 and Sep 17, 2026 — classified as 9 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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 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.

• InjurySep 17, 2026Adverse Event Without Identified Device or Use Problem

  Patient problems: Unspecified Infection

  MAUDE report 50810918 ↗
• InjuryJul 13, 2026Device Dislodged or Dislocated

  IT WAS REPORTED THAT SURGEON REMOVED A 42 +6 HUMERAL CUP AND A 42 + 6 LATERALIZED GLENOSPHERE BECAUSE PATIENT WAS DISLOCATING AND PUT IN A 42 + 8 GLENOSPHERE AND A +9 HUMERAL SPACER AND A 42 +3 HUMERAL CUP. DOI: (B)(6) 2025 DOR: (B)(6) 2026 AFFECTED SIDE: RIGHT SHOULDER.

  Patient problems: Joint Dislocation

  MAUDE report 25796837 ↗
• InjuryJul 9, 2026Device Dislodged or Dislocated

  IT WAS REPORTED THAT REMOVED A 42 +6 HUMERAL CUP AND A 42 + 6 LATERALIZED GLENOSPHERE BECAUSE PATIENT WAS DISLOCATING AND PUT IN A 42 + 8 GLENOSPHERE AND A +9 HUMERAL SPACER AND A 42 +3 HUMERAL CUP. AFFECTED SIDE- RIGHT SHOULDER.

  Patient problems: Joint Dislocation

  MAUDE report 25764577 ↗
• InjurySep 16, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated

  PATIENT WAS DISLOCATING SO SURGEON SWAPPED PARTS. DOI: UNKNOWN. DOR: (B)(6) 2025. AFFECTED SIDE: RIGHT SHOULDER.

  Patient problems: Joint Dislocation

  MAUDE report 23066179 ↗
• InjurySep 4, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT PATIENT IS CHRONICALLY UNSTABLE. SURGEON CHANGED GLENOSPHERE AND POLY IN AN ATTEMPT TO MAKE THEM MORE STABLE. AFFECTED SIDE: LEFT SHOULDER.

  Patient problems: Joint Laxity

  MAUDE report 22964228 ↗
• InjuryAug 7, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED DUE TO INFECTION. ALL PARTS WERE EXPLANTED. AFTER WASH OUT NEW PARTS WERE IMPLANTED. NO SURGICAL DELAY. NO PATIENT CONSEQUENCE. DOI: (B)(6) 2023, DOR: (B)(6) 2025, AFFECTED SIDE: RIGHT SHOULDER.

  Patient problems: Unspecified Infection

  MAUDE report 22743440 ↗
• InjuryApr 19, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT PATIENT WAS REVISED DUE TO DISLOCATED SHOULDER. DOI: (B)(6) 2022. DOR: (B)(6) 2024. AFFECTED SIDE: UNKNOWN.

  Patient problems: Joint Dislocation

  MAUDE report 19144117 ↗
• InjuryNov 6, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated

  PATIENT WAS REVISITED FOR DISLOCATION. IT WAS UNKNOWN ABOUT SURGICAL DELAY. DOI: UNKNOWN. DOR: UNKNOWN. AFFECTED SIDE: UNKNOWN.

  Patient problems: Joint Dislocation

  MAUDE report 18073364 ↗
• InjuryMar 13, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT WAS REVISED TO ADDRESS A DRAINING WOUND. SURGEON ELECTED TO PERFORM AN I&D WITH GLENOSPHERE, POLY, AND SPACER EXCHANGE. NO LOOSENING AND NO SURGICAL DELAY REPORTED. DOI: (B)(6) 2020. DOR: (B)(6) 2020, RIGHT SHOULDER.

  Patient problems: No Code Available

  MAUDE report 9831027 ↗