DELTA XTEND 2307-77-003Recalls & reported problems
Depuy (Ireland) · DELTA Xtend EPIPHYSEAL DISK FOR MODULAR IMPLANT SZ 1 · Class 1
All models of DELTA XTEND (194)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295116226), received between Oct 23, 2017 and Jun 8, 2026 — classified as 1 injury, 3 malfunctions.
The most frequently reported specific device problem is “Device-Device Incompatibility” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Device-Device Incompatibility2
- Appropriate Device Problem Term/Code Not Available1
- Break1
- Material Deformation1
- Material Integrity Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- No Consequences Or Impact To Patient2
- No Information1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 8, 2026Break
IT WAS REPORTED THAT DURING A SHOULDER REPAIR SURGERY, THE GREEN DISK WAS BROKEN AND THROWN AWAY AFTER THE CASE. THE BLUE HANDLE SCREWDRIVER WAS STRIPPED. THE HUMERAL CUPS WERE ALSO BROKEN AND THROWN AWAY AFTER THE CASE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25429348 ↗MalfunctionOct 31, 2025Device-Device Incompatibility; Material Deformation; Material Integrity Problem; Device-Device Incompatibility; Material Deformation; Material Integrity Problem
ADDITIONAL INFORMATION RECEIVED: THE PRODUCT WAS WARPED FROM REPEATED USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23439129 ↗MalfunctionAug 30, 2019Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE TIP OF INTERNAL ROD WAS BROKEN AND THROWN AWAY. GREEN SIZING DISC WOULD NOT FIT OVER ADAPTER. DID NOT IMPACT CASE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8951689 ↗InjuryOct 23, 2017Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
COMPLAINT DESCRIPTION: IT WAS REPORTED THAT THE EPI 1 TOP HAT WOULD NOT FILL OVER THE SLEEVES AND GOT STUCK DURING SURGERY. INVESTIGATION METHOD: NOVEMBER 14, 2017: COMPLAINT SAMPLE DEVICES SHIPPED BY (B)(6). AWB# TO BE DETERMINED. CAUGHELL INVESTIGATION SUMMARY: IT WAS REPORTED THAT THE EPI 1 TOP HAT WOULD NOT FILL OVER THE SLEEVES AND GOT STUCK DURING SURGERY.
Patient problems: No Consequences Or Impact To Patient; No Information
MAUDE report 6968308 ↗
Other TEMPLATE devices
- ATTUNE 2544-01-014Depuy (Ireland) · TEMPLATE802 reports
- ATTUNE 2545-00-546Depuy (Ireland) · TEMPLATE1 recall301 reports
- ARTICUL/EZE 2531-51-000Depuy (Ireland) · TEMPLATE323 reports
- DELTA XTEND 2307-95-000Depuy (Ireland) · TEMPLATE315 reports
- ATTUNE 2545-00-547Depuy (Ireland) · TEMPLATE1 recall231 reports
- ATTUNE 2544-00-520Depuy (Ireland) · TEMPLATE279 reports
- ATTUNE 2545-00-545Depuy (Ireland) · TEMPLATE1 recall221 reports
- ARTICUL/EZE 2530-91-000Depuy (Ireland) · TEMPLATE271 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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