GLOBAL STEPTECH APG 2230-00-066Recalls & reported problems
Depuy Orthopaedics, Inc. · GLOBAL STEPTECH APG PERIPHERAL DRILL GUIDE +5mm RIGHT · Class 1
All models of GLOBAL STEPTECH APG (12)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295103394), received between Sep 24, 2021 and Sep 24, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Failure to Cut” (1 report).
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
- Failure to Cut1
- Naturally Worn1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 24, 2021Failure to Cut; Naturally Worn; Failure to Cut; Naturally Worn
SURGEON WAS DOING A STEPTECH GLENOID, AND WHILE USING THE RASP GUIDE, NOTICED THAT IT WAS WORN DOWN IN THE AREA THAT THE RASP SITS AGAINST. THIS IN TURN CAUSED THE RASPS TO NOT SHAVE OFF BONE CORRECTLY. WAS SURGERY DELAYED DUE TO THE REPORTED EVENT? YES. IF YES, NUMBER OF MINUTES: 15. ACTION TAKEN WHEN EVENT OCCURRED? SURGEON HAD TO USE A BURR TO CLEAN UP THE AREA WHERE THE RASP DID NOT DEBRIDE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12528424 ↗
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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