Tiger 200-30-030Recalls & reported problems
Trilliant Surgical, LLC · 3.0mm x 30mm Tiger Cannulated Screw · Class 2 · Implant
All models of Tiger (20)
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 00812926021027), received between May 30, 2017 and May 30, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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 Dislodged or Dislocated1
Patient problems
- Edema1
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 30, 2017Device Dislodged or Dislocated
A PATIENT CAME BACK INTO THE DOCTORS OFFICE TO REPORT PAIN IN HER FOOT. THE DOCTOR X-RAYED HER FOOT AND NOTICED THAT THE SCREWS WERE DISLOCATED FROM THE FUSION SITE. THE DOCTOR SUSPECTS NON-COMPLIANCE AND DECIDED TO REMOVE THE TWO TIGER CANNULATED SCREWS ON (B)(6) 2017. THE TWO SCREWS WERE REMOVED WITHOUT ANY DIFFICULTY. THE DOCTOR DID NOT PUT ANY OTHER HARDWARE BACK IN THE PATIENT ON (B)(6) 2017 AS THE PATIENT HAD EDEMA AND HE DID NOT WANT TO FURTHER IRRITATE THE SITE.
Patient problems: Edema; Pain
MAUDE report 6598045 ↗
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- HEALIX PEEK ORTHOCORD 222205Medos International Sàrl · Screw, fixation, bone186 reports
- PRECICE® Bone Transport System STP3.5-350Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-400Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-300Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-200Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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