Arthrex® AR-VIP3DRecalls & reported problems
Arthrex, Inc. · VIP GLENOID 3D MODEL · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867335769), received between Oct 23, 2020 and Oct 23, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Device-Device Incompatibility” (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 16, 2026.
Most reported problems
Device problems
- Device-Device Incompatibility1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 23, 2020Device-Device Incompatibility
IT WAS REPORTED, THAT THE AR-VIP3D MODEL AND THE TARGETED LEGS DID NOT MATCH UP AT ALL. THE SURGEON WAS NOT PLEASED WITH THIS PLAN. THE REP REPORTED IT WAS ALMOST LIKE THE MODEL ANATOMY DID NOT MATCH THE PATIENTS. THE MODEL IS RETURNING. ADDITIONAL INFORMATION RECEIVED ON 10/6/2020: THE REP REPORTED THE SURGERY WAS NOT RESCHEDULED BUT THE ISSUE WITH THE MODEL CAUSED THE SURGEON TO HAVE TO FREEHAND THE GUIDE PIN.
Patient problems: Insufficient Information
MAUDE report 10730523 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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