PINNACLE 2274-70-800Recalls & reported problems

Summary

The FDA's MAUDE database contains 11 adverse event reports that list this exact device (DI 10603295109419), received between Feb 28, 2019 and Feb 2, 2026 — classified as 11 malfunctions.

The most frequently reported specific device problem is “Break” (10 reports).

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 11 most recent of 11 reports, in the reporter's own words as published by the FDA.

• MalfunctionFeb 2, 2026Break

  IT WAS REPORTED THAT THE DRILL BROKE DURING NORMAL USE. THE BROKEN PIECE WAS RETRIEVED AND THE DRILL WAS DISPOSED OF. A DIFFERENT DRILL FROM THE SET WAS USED TO COMPLETE THE SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24232816 ↗
• MalfunctionJan 29, 2026Break

  IT WAS REPORTED THAT DURING A PROCEDURE THE DRILL BROKE. THE BROKEN PIECE WAS RETRIEVED AND BOTH PIECES WERE DISPOSED OF IN THEATRE. A DIFFERENT DRILL FROM THE SET WAS USED TO COMPLETE THE CASE AND THERE WAS NO ADVERSE CONSEQUENCE FOR THE PATIENT. THERE WAS NO SURGICAL DELAY DUE TO THE REPORTED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24210261 ↗
• MalfunctionJul 18, 2025Break; Break

  IT WAS REPORTED THE DEVICES WERE BROKEN.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22544041 ↗
• MalfunctionJul 17, 2025Break; Break

  IT WAS REPORTED THAT THERE WAS BREAKAGE AND REPAIR OF CONSIGNED ITEMS IN THE ACCOUNT FROM GENERAL USAGE. NO OTHER INFORMATION WAS PROVIDED AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22532375 ↗
• MalfunctionJul 17, 2025Break; Break

  IT WAS REPORTED THAT THERE WAS BREAKAGE AND REPAIR OF CONSIGNED ITEMS IN THE ACCOUNT FROM GENERAL USAGE. NO OTHER INFORMATION WAS PROVIDED AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22532358 ↗
• MalfunctionFeb 7, 2024Break; Break

  IT WAS REPORTED THAT THE TWO DRILL BITS ARE BROKEN.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18660681 ↗
• MalfunctionNov 13, 2023Break; Break

  IT WAS REPORTED THAT TRIAL LINERS, SCREW BIT HAS COME OFF, DOME DRILLS TIP WAS BROKEN. THERE WAS NO PATIENT CONSEQUENCE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18124869 ↗
• MalfunctionNov 13, 2023Break; Break

  ADDITIONAL INFORMATION WAS RECEIVED: A. DID IT BROKE INTO TWO OR MORE PIECES? 2 PIECES. B. WERE THERE ANY FRAGMENTS GENERATED? IF YES, WERE ALL THE PIECES RETRIEVED? NO FRAGMENTS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18124510 ↗
• MalfunctionDec 8, 2022Break; Break

  IT WAS REPORTED THAT THE DRILL BROKE DURING KNEE SURGERY TODAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15939176 ↗
• MalfunctionJun 11, 2021Break; Break

  IT WAS REPORTED THAT THE TIP OF THE DRILL BIT BROKE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11986323 ↗
• MalfunctionFeb 28, 2019Dull, Blunt; Dull, Blunt

  IT WAS REPORTED THAT THE DRILL BITS WAS DULL FROM REGULAR USE. NO SURGERY AND IT WAS..

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8378953 ↗