Tiger 201-40-040Recalls & reported problems
Trilliant Surgical, LLC · 4.0mm x 40mm 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 00810028392854), received between Mar 11, 2025 and Mar 11, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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
- Detachment of Device or Device Component1
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 11, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
COMPLAINT: DOCTOR WAS FUSING A LIZ FRANK INJURY UTILIZING AN ENOVIS 4.0 CANNULATED SCREW. AFTER PUTTING IN THE K WIRE AND USING THE APPROPRIATE PILOT DRILL HE BEGAN INSERTING THE SCREW USING A MANUAL SCREWDRIVER. WHEN THE THREADS WERE ABOUT HALFWAY THROUGH THE JOINT THE SCREW SNAPPED AT THE JUNCTION OF THE CORE AND THE THREADS. THERE WAS A 1-HOUR DELAY IN THE CASE. TO GET THE BROKEN PORTION OF THE SCREW OUT DOCTOR HAD TO TRY FINE OVER THE SCREW LEFT IN THE PATIENT AND THEN TAMP THE THREADED PORTION OUT WHICH CAUSED SIGNIFICANT REMOVAL OF BONE IN THAT PORTION OF THE PATIENT'S FOOT.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 21580007 ↗
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- PRECICE® Bone Transport System STP3.5-350Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
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- 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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