Tiger 200-24-020Recalls & reported problems
Trilliant Surgical, LLC · 2.4mm x 20mm 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 00812926020778), received between Dec 23, 2019 and Dec 23, 2019 — 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
- Foreign Body In Patient1
- Skin Irritation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 23, 2019Migration or Expulsion of Device; Migration or Expulsion of Device
ON 11/27/2019, AN R.LPN EMAILED [email protected] THE FOLLOWING: "HELLO, DOCTOR 1 IS A PODIATRIST AT FACILITY X. HE IS IN NEED OF A SCREWDRIVER FOR A SURGICAL HARDWARE REMOVAL CASE IN FACILITY Y. HERE IS THE INFORMATION ON THE SCREW: IMP SCR TRILLIANT CAN TIGER 2.4X20MM TI - IMPLANTED (LEFT) TOE . INVENTORY ITEM: IMP SCR TRILLIANT CAN TIGER 2.4X20MM TI 200-24-020 . MODEL/CAT NUMBER: 200-24-020 MANUFACTURER: TRILLIANT SURGICAL. PLEASE LET US KNOW HOW WE CAN OBTAIN THIS SCREWDRIVER. DOCTOR 1 CAN BE REACHED AT [PHONE NUMBER] FOR ANY FOLLOW UP QUESTIONS. THANKS MUCH! X R.LPN". A TRILLIANT SURGICAL SALES SUPPORT SPECIALIST FOLLOWED UP ON 11/27/2019 VIA PHONE CALL AND ASKED FOR FURTHER DETAILS REGARDING THE REMOVAL. DOCTOR 1 STATED THAT THE REMOVAL WILL BE HAPPENING ON (B)(6) 2019 AT 3:30PM AT FACILITY Y (NOT A CURRENT TRILLIANT SURGICAL CUSTOMER AS OF (B)(6) 2019). DOCTOR 1 REPORTED THAT THE 37-YEAR-OLD FEMALE PATIENT STATED THAT SHE ORIGINALLY HAD THE 2.4MM X 20MM TIGER CANNULATED SCREW (200-24-020) IMPLANTED A "FEW MONTHS PRIOR IN [A DIFFERENT STATE]". DOCTOR 1 STATED THAT THE PATIENT CAME IN REPORTING THAT THE SCREW HAD BECOME SUPERFICIALLY VISIBLE AS THE SWELLING AT THE SUR
Patient problems: Foreign Body In Patient; Skin Irritation
MAUDE report 9513403 ↗
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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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