GLOBAL APG+ 2236-00-019Recalls & reported problems
Depuy (Ireland) · GLOBAL APG+ TRIAL SIZE 44 · Class 1
All models of GLOBAL APG+ (34)
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 10603295105862), received between Oct 26, 2017 and Aug 7, 2023 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Break” (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 18, 2026.
Most reported problems
Device problems
- Break3
- Material Twisted/Bent1
- Scratched Material1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- No Consequences Or Impact To Patient1
- No Information1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 7, 2023Break; Scratched Material; Break; Scratched Material
DEVICE REPORT FROM DEPUY SYNTHES AUSTRALIA REPORTS AN EVENT AS FOLLOWS: DURING A LOAN KIT INSPECTION IT WAS DISCOVERED THAT THE PLASTIC HOLES IN THE TRIAL 44 SHOW GOUGES AND ARE SHREDDED FROM DRILL BITS. NO FURTHER INFORMATION AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17470500 ↗MalfunctionFeb 15, 2021Break; Break
IT WAS REPORTED THAT A PERIPHERAL PEG ON THE TRIAL GLENOID BROKE OFF DURING USE. ALL PIECES WERE RETRIEVED FROM PATIENT AND NO SURGICAL DELAY WAS CAUSED. IT DID BREAK INTO 2 SEPARATE PIECES. THE MAIN BODY OF TRIAL IS STILL INTACT, BUT THE BOTTOM PERIPHERAL PEG THAT WAS BROKEN OFF WAS AND MISTAKENLY THROWN AWAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11329690 ↗MalfunctionSep 13, 2019Material Twisted/Bent; Material Twisted/Bent
IT WAS REPORTED THAT THE TRIAL HAS EXCESSIVE WEAR DUE TO TRIALING. NOTHING LEFT IN PATIENT AND NO SURGICAL DELAY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9027898 ↗MalfunctionOct 26, 2017Break; Break
IT WAS REPORTED THAT THE BOTTOM PEG ON THE 44 GLENOID TRIAL CAME OFF.
Patient problems: No Information
MAUDE report 6981333 ↗
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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