Tiger 200-24-024Recalls & reported problems
Trilliant Surgical, LLC · 2.4mm x 24mm Tiger Cannulated Screw · Class 2
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 00812926020792), received between Jun 3, 2021 and Jun 3, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Migration or Expulsion of Device” (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
- Migration or Expulsion of Device1
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.
InjuryJun 3, 2021Migration or Expulsion of Device; Migration or Expulsion of Device
ON (B)(6) 2021 , A TRILLIANT SURGICAL INDEPENDENT SALES REPRESENTATIVE CALLED A DJO SALES SUPPORT SPECIALIST TO REPORT OF A MIB REMOVAL DUE TO PATIENT PAIN THAT OCCURRED ON (B)(6) 2021 AT FACILITY 1 WITH DOCTOR 1 FOR A (B)(6) YEAR-OLD FEMALE PATIENT (DOB (B)(6) , WEIGHT UNKNOWN). THE ORIGINAL IMPLANTATION ALSO OCCURRED AT FACILITY 1, ON (B)(6) 2020 BY DOCTOR 1. THE SALES REPRESENTATIVE REPORTED THAT THE MIB CONSTRUCT WAS REMOVED BECAUSE THE 200-24-024 (2.4MM X 24MM TIGER CANNULATED SCREW), UTILIZED AS THE INTERFRAG SCREW, DID NOT ACHIEVE COMPRESSION AT THE SURGICAL SITE AND BEGAN TO "BURY ITSELF" WITHIN THE PLATE SCREW HOLE. THE ENTIRE CONSTRUCT (200-24-020 (2.4MM X 20MM TIGER CANNULATED SCREW), 200-24-024 (2.4MM X 24MM TIGER CANNULATED SCREW), 300-70-002 (MINIMALLY INVASIVE BUNION PLATE, LEFT), 302-24-018 (2.4MM X18MM GL LOCKING SCREW)) WAS REMOVED AFTER DOCTOR 1 HAD TO BURR THE ENTIRE 200-24-024 SCREW HEAD TO BE ABLE TO LIFT THE PLATE OFF THE SURGICAL SITE. IT IS TO BE NOTED THAT THE BUNION HAD BEEN CORRECTED AND NO FURTHER SURGICAL INTERVENTION WAS REQUIRED. ALL ASSOCIATED PARTS WITH THE REMOVAL WERE RETAINED BY THE FACILITY AND WILL NOT BE RETURNED TO CORPORATE FOR FURTHER REVI
Patient problems: Pain
MAUDE report 11929690 ↗
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- 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 13, 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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