Delta Xtend 1309-60-010Recalls & reported problems
Depuy (Ireland) · Delta Xtend REVERSE SHOULDER SYSTEM CENTRAL SCREW METAGLENE +10mm PEG · Class 2 · Implant
All models of DELTA XTEND (194)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295525134), received between Mar 13, 2024 and Mar 13, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Difficult to Advance” (1 report).
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.
Reports received per month
Most reported problems
Device problems
- Difficult to Advance1
- Naturally Worn1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 13, 2024Difficult to Advance; Naturally Worn; Difficult to Advance; Naturally Worn
IT WAS REPORTED THAT THE GLENOSPHERE SCREW WOULD NOT LOCK INTO THE METAGLENE COLLET. EVERYTHING WAS IMPLANTED AND USED ACCORDING THE THE SURGICAL TECHNIQUE, BUT WHEN THE SURGEON WENT TO TIGHTENT THE SCREW INTO THE METAGLENE IT ACTED AS IF IT WAS STRIPPED. A GOOD BITE WAS NOT ATTAINABLE AND THE SCREW WOULD JUST KEEP SPINNING AND NOT ENGAGE INTO THE COLLET. ANY EXCESS BONE WAS REMOVED AROUND THE METAGLENE, SO THE SURGEON DID NOT SEE ANY INTERFERENCE WITH THE HEAD. THE GLENOSPHERE HAD GOOD FIXATION VIA THE MORSE TAPER ONTO THE METAGLENE, SO THE SURGEON LEFT IT AS THAT WITHOUT TIGHTENING THE SCREW.
Patient problems: Insufficient Information
MAUDE report 18892939 ↗
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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