CORE Shoulder System 87-9136Recalls & reported problems
Link Bio Corp · Workstation · Class 2
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00810022403099), received between Mar 6, 2026 and Mar 6, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Displays Incorrect Message” (1 report).
1 FDA recall record name this device's identifier, 1 still open.
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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Recalls naming this device
- Mar 12, 2026Open, Classified
The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.
Z-1810-2026 · Root cause: Under Investigation by firm · FDA record ↗
Most reported problems
Device problems
- Device Displays Incorrect Message1
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.
MalfunctionMar 6, 2026Device Displays Incorrect Message
TWO CORE WORKSTATIONS IN INVENTORY WERE FOUND TO HAVE OUT-OF-SYNC TIME/DATE. AN ENGINEER LOGGED INTO THE SERVICE ACCOUNT FOR EACH WORKSTATION TO VIEW THE TIME AND DATE DISPLAYED ON THE TABLET'S CLOCK AND THEY WERE OBSERVED TO BE OUT-OF-SYNC BY SEVERAL MONTHS. AN ENGINEER THEN RE-SYNCED THESE WORKSTATIONS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24539180 ↗
Other Shoulder Arthroplasty Implantation System devices
- 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
- Arthrex® 5566VIPArthrex, 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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.