GLOBAL APG+ 2236-21-000Recalls & reported problems
Depuy (Ireland) · GLOBAL APG+ GLENOID IMPACTOR TIP · Class 1
All models of GLOBAL APG+ (34)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10603295106128), received between Oct 11, 2018 and Nov 18, 2025 — classified as 7 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
- Material Deformation2
- Material Twisted/Bent2
- Naturally Worn2
- Scratched Material1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
- No Consequences Or Impact To Patient3
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 18, 2025Device-Device Incompatibility; Material Deformation; Device-Device Incompatibility; Material Deformation
IT WAS REPORTED THAT THREADS ON THE APG INSERTER TIP WERE STRIPPED AND WOULD NOT TIGHTEN ONTO HANDLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23586783 ↗MalfunctionFeb 26, 2024Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THE IMPACTOR TIP WAS STRIPPED. SURGICAL DELAY WAS UNKNOWN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18776884 ↗MalfunctionJul 18, 2023Device-Device Incompatibility; Naturally Worn; Device-Device Incompatibility; Naturally Worn
IT WAS REPORTED THAT THE IMPACTOR TIP WONT THREAD INTO HANDLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17341925 ↗MalfunctionAug 17, 2021Scratched Material; Scratched Material
IT WAS REPORTED THAT THE GLENOID PUSHER HAS BECOME SCRATCHED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12331831 ↗MalfunctionMar 13, 2020Material Twisted/Bent; Material Twisted/Bent
IT WAS REPORTED THAT THE IMPACTOR TIP THREADS WERE STRIPPED. NO SURGICAL DELAY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9831094 ↗MalfunctionFeb 4, 2020Material Twisted/Bent; Material Twisted/Bent
IT WAS REPORTED THAT THE THREADING IS STRIPPED AND IT NEEDS TO BE REPLACED. NO SURGICAL DELAY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9667712 ↗MalfunctionOct 11, 2018Material Deformation; Material Deformation
IT WAS REPORTED THAT THE WHITE PLASTIC TIP FOR IMPACTING THE ANCHOR PEG GLENOID IMPLANT WILL NOT THREAD ONTO THE HANDLE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7956800 ↗
Other IMPACTOR devices
- PINNACLE 2217-50-041Depuy (Ireland) · IMPACTOR4,295 reports
- ATTUNE 2544-01-006Depuy (Ireland) · IMPACTOR1 recall2,539 reports
- ATTUNE 2544-01-003Depuy (Ireland) · IMPACTOR1 recall1,498 reports
- ATTUNE 2544-01-017Depuy (Ireland) · IMPACTOR1 recall1,456 reports
- ATTUNE 2544-01-004Depuy (Ireland) · IMPACTOR1 recall875 reports
- DURALOC 2360-71-000Depuy Orthopaedics, Inc. · IMPACTOR716 reports
- SPECIALIST 2581-11-000Depuy (Ireland) · IMPACTOR704 reports
- INHANCE 6205-10-103Depuy (Ireland) · IMPACTOR337 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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