INHANCE 6507-24-100Recalls & reported problems
Depuy (Ireland) · INHANCE SHOULDER SYSTEM KICKSTAND GUIDE SMALL Ø24 · Class 1
All models of INHANCE (202)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295549697), received between Oct 7, 2024 and Apr 16, 2026 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Device-Device Incompatibility” (4 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 Incompatibility4
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 16, 2026Device-Device Incompatibility
IT WAS REPORTED THAT PILOT ROD GOT STUCK IN SMALL KICKSTAND GUIDE, COULD NOT BE REMOVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24895627 ↗MalfunctionJul 7, 2025Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE GUIDE AND DRILL WERE GETTING STUCK TOGETHER. THE PATIENT WAS NOT AFFECTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22413240 ↗MalfunctionJan 31, 2025Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT AFTER THE CASE STERILE PROCESSING DEPARTMENT (SPD) INFORMED THAT THEY COULDN'T GET THE MILL OUT OF THE KICKSTAND GUIDE. CUSTOMER TRIED TO GET IT OUT AND ALSO FAILED TO GET OUT OF THE GUIDE. DUE TO IT NOT BEING ABLE TO BE PROPERLY GUIDE, SPD DISPOSED OF THE ITEMS PER THEIR POLICY. THERE WAS NO PATIENT CONSEQUENCE AND NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21284541 ↗MalfunctionOct 7, 2024Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT AFTER THE CASE THE TECH SHOWED SALES REP THAT THE MILL WAS STUCK INSIDE THE THE LARGE KICKSTAND GUIDE. SALES CONSULTANT WAS ABLE TO REMOVE IT AFTER THE PROCEDURE BUT WHILE CHECKING THE INSTRUMENTS TO MAKE SURE THEY WOULD STILL PREFORM CORRECTLY. UNFORTUNATELY THE MILL DIDN¿T SEEM TO FULLY SEAT INTO EITHER THE LARGE OR THE SMALL KICKSTAND GUIDE. ALL 3 ITEMS HAVE BEEN REMOVED FROM THE SET UNTIL REPLACED. THERE WAS NO DELAY TO THE SURGERY NOR WAS THERE ANY NEGATIVE IMPACT TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20390914 ↗
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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