Tiger 200-30-018Recalls & reported problems
Trilliant Surgical, LLC · 3.0mm x 18mm 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 00812926020969), received between May 26, 2021 and May 26, 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.
InjuryMay 26, 2021Insufficient Device Problem Information; Insufficient Device Problem Information
ON 04/28/2021, A MATERIALS MANAGER AT FACILITY 1 CALLED A TRILLIANT SURGICAL SALES SUPPORT SPECIALIST TO REQUEST A 200-30-018 (3.0MM X 18MM TIGER CANNULATED SCREW) REMOVAL KIT FOR AN UPCOMING REMOVAL WITH DOCTOR 1 AT FACILITY 1 ON (B)(6) 2021 WITH A FEMALE PATIENT. IT IS TO BE NOTED THAT PATIENT PAIN WAS REPORTED DURING POST-OP REVIEW. THE MATERIALS MANAGER NOTED THE ORIGINAL IMPLANTATION OCCURRED ON (B)(6) 2012 AT FACILITY 2 BY DOCTOR 2. FURTHER DETAILS WILL BE OBTAINED IN AN INTERVIEW POST REMOVAL.
Patient problems: Pain
MAUDE report 11887337 ↗
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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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