Tiger 200-30-024Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00812926020990), received between Mar 3, 2021 and Mar 3, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Patient Device Interaction Problem” (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

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryMar 3, 2021Patient Device Interaction Problem; Patient Device Interaction Problem

  ON (B)(6) 2021, A TRILLIANT SURGICAL INDEPENDENT SALES REPRESENTATIVE SENT IN A FIELD INCIDENT REPORT (FIR) WITH A 200-30-024 (3.0MM X 24MM TIGER CANNULATED SCREW) TO TRILLIANT SURGICAL CORPORATE. A TRILLIANT SURGICAL SALES SUPPORT SPECIALIST CALLED THE SALES REPRESENTATIVE TO OBTAIN FURTHER DETAILS FOR THE PART RETURN AND FIR FORM. THE SALES REPRESENTATIVE STATED THAT ON (B)(6) 2021, DOCTOR 1 HAD SCHEDULED A REMOVAL AT FACILITY 1, ON A (B)(6)-YEAR-OLD FEMALE PATIENT (DOB AND PATIENT WEIGHT REMAINS UNKNOWN AFTER REVIEW OF CASE WRITE UP) WHO WAS EXPERIENCING LOCALIZED PAIN / IRRITATION ON HER RIGHT FOOT. IT IS UNKNOWN WHEN THE PAIN INITIALLY BEGAN WITH THE PATIENT, HOWEVER, DOCTOR 1 SCHEDULED TO REMOVE THE PREVIOUS HARDWARE ORIGINALLY IMPLANTED. THE ORIGINAL IMPLANTATION OCCURRED ON (B)(6) 2020 AND THE SALES REPRESENTATIVE RECALLED THAT DOCTOR 1 PERFORMED A CHEILECTOMY / 1ST MPJ ARTHROPLASTY WITH A 101-00-002 (3S HEMI IMPLANT, MEDIUM, NON-STERILE) WHILE ALSO INSERTING A 200-30-024 (3.0MM X 24MM TIGER CANNULATED SCREW) TO FIXATE THE PATIENT'S BUNION. THE SURGERY WAS REPORTED TO BE SUCCESSFUL. AT TIME OF REMOVAL, DOCTOR 1 NOTICED THE 200-30-024 WAS INTERFERING WITH THE PATIENT'S SESAM

  Patient problems: Pain

  MAUDE report 11406300 ↗