Tiger 200-45-140Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00812926028989), received between Nov 30, 2022 and Nov 30, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (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.

• InjuryNov 30, 2022Break; Break

  ON (B)(6) 2022, AN INDEPENDENT SALES REPRESENTATIVE, EMAILED THE COMPLAINTS INBOX TO REPORT A COMPLAINT OF A 200-45-140 (4.5MM X 40MM LTTCS) WHICH BROKE DURING A CASE AT HOSPITAL 1 - WITH DR. 1. THE INDEPENDENT SALES REPRESENTATIVE STATED IN HIS EMAIL "JUST HAD A TIGER 4.5 LONG THREAD BREAK WHILE INSERTING UNDER HEAVY PRESSURE ON SUPER HARD BONE" AND THAT "WE GOT THE HEAD OUT (PICTURE) LEAVING THREADED DISTAL END IN SINCE IT'S ACROSS THE JOINT." BRAD PROVIDED PHOTOS OF THE INTRA-OPERATIVE X-RAY AND REMOVED BROKEN 200-45-140 SCREW HEAD.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 15891066 ↗