DELTA XTEND 1307-64-042Recalls & reported problems
Depuy (Ireland) · DELTA XTEND Lateralized Glenosphere +4mm Eccentric 042mm · Class 2 · Implant
All models of DELTA XTEND (194)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 7
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 10603295502487), received between Nov 30, 2020 and Jan 6, 2026 — classified as 7 injuries, 2 malfunctions.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (3 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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem4
- Device Dislodged or Dislocated3
- Difficult to Insert2
Patient problems
- Joint Dislocation3
- Unspecified Infection3
- No Clinical Signs, Symptoms or Conditions2
- Joint Laxity1
- Unspecified Tissue Injury1
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
InjuryJan 6, 2026Adverse Event Without Identified Device or Use Problem
PATIENT WAS REVISED DUE TO INFECTION. IT WAS STATED THAT THE METEGLENE WAS LOOSE. LOOSENING INTERFACE WAS MARKED AS BONE TO IMPLANT INTERFACE. NO ADDITIONAL INFORMATION. DOI: (B)(6) 2025. DOR: (B)(6) 2025. AFFECTED SIDE: RIGHT.
Patient problems: Unspecified Infection
MAUDE report 23976515 ↗InjuryMay 3, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
PATIENT WAS REVISED DUE TO UNKNOWN REASON. DOI: (B)(6) 2023, DOR: (B)(6) 2023, AFFECTED SIDE: UNKNOWN SHOULDER.
Patient problems: Unspecified Infection
MAUDE report 16859761 ↗InjuryMar 8, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
PATIENT WAS REVISED DUE TO INFECTION. ALL COMPONENTS REMOVED, TEMPORARY SPACER WAS IMPLANTED UNTIL INFECTION IS CLEARED. THERE WAS NO SURGICAL DELAY. DOI: (B)(6) 2022. DOR: (B)(6) 2022. AFFECTED SIDE: RIGHT SHOULDER.
Patient problems: Unspecified Infection
MAUDE report 16502664 ↗InjuryDec 1, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated
PATIENT DISCLOCATED DUE TO SIGNIFICANT SOFT TISSUE LOSS FROM PREVIOUS INJURY. POLY AND GLENOSPHERE AND SCREW EXCHANGED TO IMPROVE FIXATION TO DEAL WITH HIGHER OFFSET GLOENOSPHERE.
Patient problems: Joint Dislocation; Unspecified Tissue Injury
MAUDE report 15895492 ↗InjuryAug 18, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated
PATIENT WAS REVISED DUE TO DISLOCATION. NEW GLENOSPHERE IMPLANTED. NO FURTHER INFORMATION AVAILABLE. THERE WAS NO REPORTED LOOSENING. THERE WAS NO SURGICAL DELAY. DOI: (B)(6) 2022. DOR: (B)(6) 2022. AFFECTED SIDE: RIGHT SHOULDER.
Patient problems: Joint Dislocation
MAUDE report 15248920 ↗InjuryMay 4, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE PATIENT WAS REVISED DUE TO INSTABILITY. THERE WAS NO LOOSENING. THERE WAS NO SURGICAL DELAY. DOI: (B)(6) 2020; DOR: (B)(6) 2022; AFFECTED SIDE: RIGHT SHOULDER.
Patient problems: Joint Laxity
MAUDE report 14278860 ↗InjuryFeb 11, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated
PATIENT WAS REVISED DUE TO DISLOCATION. THERE WAS NO SURGICAL DELAY REPORTED. DOI: UNKNOWN. DOR: (B)(6) 2022. AFFECTED SIDE: RIGHT SHOULDER.
Patient problems: Joint Dislocation
MAUDE report 13514892 ↗MalfunctionJan 6, 2021Difficult to Insert; Difficult to Insert
IT WAS REPORTED THAT COULD NOT GET GLENOSPHERE TO ENGAGE TO METAGLENE. OPENED ANOTHER GLENOSPHERE PER SURGEON REQUEST AND THAT ONE DID ENGAGE AND LOCK.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11123150 ↗MalfunctionNov 30, 2020Difficult to Insert; Difficult to Insert
IT WAS REPORTED THAT THE GLENOSPHERE WOULD NOT LOCK DOWN COMPLETELY ONTO METAGLENE. NO SURGICAL DELAY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 10920122 ↗
Other shoulder prosthesis, reverse configuration devices
- DJO SURGICAL 508-36-101Encore Medical, L.P. · shoulder prosthesis, reverse configuration508 reports
- DJO SURGICAL 508-32-101Encore Medical, L.P. · shoulder prosthesis, reverse configuration433 reports
- DJO SURGICAL 508-32-103Encore Medical, L.P. · shoulder prosthesis, reverse configuration421 reports
- DJO SURGICAL 509-00-036Encore Medical, L.P. · shoulder prosthesis, reverse configuration1 recall259 reports
- DJO SURGICAL 508-32-104Encore Medical, L.P. · shoulder prosthesis, reverse configuration1 recall203 reports
- DJO SURGICAL 509-00-032Encore Medical, L.P. · shoulder prosthesis, reverse configuration233 reports
- DELTA XTEND 130760000Depuy (Ireland) · shoulder prosthesis, reverse configuration223 reports
- DJO SURGICAL 508-00-032Encore Medical, L.P. · shoulder prosthesis, reverse configuration122 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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