GLOBAL ADVANTAGE 2236-80-090Recalls & reported problems
Depuy (Ireland) · GLOBAL ADVANTAGE ANCHOR PEG PERIPHERAL DRILL BIT · Class 1
All models of GLOBAL ADVANTAGE (28)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 8
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 10603295106319), received between Feb 21, 2019 and Jan 23, 2026 — classified as 8 malfunctions.
The most frequently reported specific device problem is “Break” (7 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
- Break7
- Dull, Blunt1
- Mechanical Jam1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- No Code Available2
- No Consequences Or Impact To Patient2
- Not Applicable2
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 23, 2026Break
IT WAS REPORTED THAT THE PERIPHERAL DRILL BIT BROKE WHILE DRILL THE LAST BEG HOLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24164431 ↗MalfunctionJan 13, 2025Break; Break
IT WAS REPORTED THAT THE PERIPHERAL DRILL THREADS BROKE OFF IN THE DRIVER HANDLE/REAMER. IT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21145069 ↗MalfunctionOct 14, 2020Break; Break
IT WAS REPORTED THAT DURING A TOTAL SHOULDER REPLACEMENT, THE ANTERIOR PEG PERIPHERAL BIT ( 223680090 ) BROKE OFF MIDWAY DOWN THE THREADS OF THE DRILL BIT, TWICE/ A DIFFERENT BITS. THE BREAK LEFT HALF OF THE THREADS IN THE GLOBAL ADVANTAGE AT DRILL DRIVER. WE CHANGED APG INSTRUMENTS. A SURGICAL DELAY OF FIVE MINUTES.
Patient problems: No Code Available
MAUDE report 10676958 ↗MalfunctionOct 14, 2020Break; Break
IT WAS REPORTED THAT DURING A TOTAL SHOULDER REPLACEMENT, THE ANTERIOR PEG PERIPHERAL BIT ( 223680090 ) BROKE OFF MIDWAY DOWN THE THREADS OF THE DRILL BIT, TWICE/ A DIFFERENT BITS. THE BREAK LEFT HALF OF THE THREADS IN THE GLOBAL ADVANTAGE AT DRILL DRIVER. WE CHANGED APG INSTRUMENTS. A SURGICAL DELAY OF FIVE MINUTES.
Patient problems: No Code Available
MAUDE report 10676957 ↗MalfunctionJul 15, 2020Break; Mechanical Jam; Break; Mechanical Jam
PERIPHERAL DRILL BIT BROKE AND THREADED PART REMAINED IN THE DRILL SHAFT. ALL PIECES WERE RETRIEVED AND THERE WAS NO DELAY IN SURGERY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10278218 ↗MalfunctionOct 21, 2019Break; Break
IT WAS REPORTED THAT THE PERIPHERAL DRILL BIT WAS BROKEN WHEN DRILLING FOR THE ANTI ROTATION PEG. SURGEON WAS DRILLING PROPERLY THROUGH THE 3 HOLE GOLD DEVICE. ALL PIECES WERE RETRIEVED. A SURGICAL DELAY OF 1 MINUTE.
Patient problems: Not Applicable
MAUDE report 9213919 ↗MalfunctionAug 26, 2019Break; Break
IT WAS REPORTED THAT WHILE DRILLING FOR THE LAST PERIPHERAL HOLE THE DRILL BIT WAS BROKEN. LEAVING SOME OF THE THREADS BROKEN OFF IN THE ST. DRIVER. TIME WASTED WAS APPROXIMATELY 5 MINUTES AS A NEW DRILL BIT WAS LOADED. NOTHING WAS LOST AND THE BROKEN.
Patient problems: Not Applicable
MAUDE report 8930282 ↗MalfunctionFeb 21, 2019Dull, Blunt; Dull, Blunt
THE FOLLOWING DRILL BITS FROM THE SET GLOBAL AP ARE REPORTED AS DULL.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8358605 ↗
Other BIT, DRILL devices
- QUICKSET 2274-25-500Depuy Orthopaedics, Inc. · BIT, DRILL1,985 reports
- QUICKSET 2274-35-500Depuy Orthopaedics, Inc. · BIT, DRILL770 reports
- QUICKSET 2274-30-500Depuy Orthopaedics, Inc. · BIT, DRILL761 reports
- NA 03.037.022Synthes GmbH · BIT, DRILL339 reports
- NA 323.062Synthes GmbH · BIT, DRILL309 reports
- QUICKSET 2274-56-000Depuy (Ireland) · BIT, DRILL275 reports
- QUICKSET 2274-45-500Depuy Orthopaedics, Inc. · BIT, DRILL211 reports
- LCS 2366-83-000Depuy (Ireland) · BIT, DRILL207 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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