Tiger 200-30-028Recalls & reported problems
Trilliant Surgical, LLC · 3.0mm x 28mm 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
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00812926021010), received between Dec 28, 2021 and Dec 28, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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
- Insufficient Device Problem Information1
Patient problems
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 28, 2021Insufficient Device Problem Information; Insufficient Device Problem Information
ON (B)(6) 2021, REPRESENTATIVE 1 FROM FACILITY 1 CALLED THE DJO ORDER MANAGEMENT TEAM TO REQUEST A REMOVAL KIT FOR A 2.0 TIGER SCREW REMOVAL CASE SCHEDULED FOR (B)(6) 2021 WITH DOCTOR 1 AT FACILITY 2 DUE TO PATIENT PAIN. ON (B)(6) 2021, DJO SALES SUPPORT MANAGER CONTACTED REPRESENTATIVE 1 TO REQUEST FURTHER INFORMATION ON THE REMOVAL CASE. REPRESENTATIVE 1 STATED THAT THE ORIGINAL IMPLANTATION SURGERY TOOK PLACE AT FACILITY 3 ON (B)(6) 2015. REPRESENTATIVE 1 STATED THE PATIENT CAME TO FACILITY 2 REPORTING OF "PAIN AND TENDERNESS WHEN PUTTING ON RIGHT SHOE ON THE 1ST MET HALLUX".
Patient problems: Pain
MAUDE report 13099214 ↗
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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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