Arthrex® 5566VIPRecalls & reported problems
Arthrex, Inc. · ArthrexVIP Web Portal · Class 2
Data updated Oct 16, 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 00888867264953), received between Jul 7, 2026 and Jul 7, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Use of Device Problem” (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.
Reports received per month
Most reported problems
Device problems
- Use of Device Problem1
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.
MalfunctionJul 7, 2026Use of Device Problem
IT WAS REPORTED THAT DURING A UNVERS REVERSE SHOULDER ARTHROPLASTY THE SURGEON DISCOVERED A DISCREPANCY BETWEEN THE PDF HAND-OUT AND THE WEB-BASED VIP PLANNING SOFTWARE. HE NOTICED THAT HE HAD PLANNED A 100% BACKSIDE SEATING AND WHEN HE OPENED THE PDF DURING THE SURGERY, HE REALIZED THAT THERE WAS SOMETHING DIFFERENT. HE DISCOVERED THAT THE STEM WAS DIFFERENT, THE SCREW LENGTHS WERE MISSING AND THE MARKING FOR THE AUGMENTED BASEPLATE HAD DISAPPEARED. AT THIS TIME, THE PATIENT WAS ALREADY UNDER ANESTHESIA. PER COMPLAINT REPORTER THERE WAS NO HARM FOR PATIENT, OPERATOR OR THIRD PARTY. THE SURGERY WAS FINISHED SUCCESSFULLY BY USING THE WEB-BASED PLANNING ON THE SIDE. THERE WAS ALSO NO DELAY IN THE SURGERY TIME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25731659 ↗
Other Shoulder arthroplasty implantation system devices
- CORE Shoulder System 87-9136Link Bio Corp · Shoulder Arthroplasty Implantation System1 recall1 report
- Blueprint BPUE001Tornier · Shoulder arthroplasty implantation system1 recall0 reports
- Blueprint BPUE001Tornier · Shoulder arthroplasty implantation system1 recall0 reports
- Comprehensive® Reverse Shoulder Augmented Guide and Bone Model Left 20-8090-004-01Orthosoft Inc · Shoulder Arthroplasty Implantation System1 report
- Comprehensive® Reverse Shoulder Augmented Guide and Bone Model Right 20-8090-004-02Orthosoft Inc · Shoulder Arthroplasty Implantation System1 report
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.
How reports and recalls are matched · Editorial policy · Report an error on this page