ATTUNE LPS 2517-60-002Recalls & reported problems

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 10603295480174), received between Jan 27, 2021 and Jan 9, 2026 — classified as 8 malfunctions.

The most frequently reported specific device problem is “Break” (6 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 18, 2026.

Most reported problems

Recent adverse event reports

The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.

• MalfunctionJan 9, 2026Break

  IT WAS REPORTED THAT THE METAL SHAVING ON THE ATTUNE REVISION LUMBAR PUNCTURE SHUNT "LPS" INSERT BASE TRIAL ADAPTER BROKE OFF.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24027595 ↗
• MalfunctionSep 2, 2025No Apparent Adverse Event; No Apparent Adverse Event

  THE INSTRUMENT WAS REPORTED FOR UNKNOWN ALLEGATION. THE EVENT DID NOT HAPPEN IN SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22938004 ↗
• MalfunctionJul 28, 2023Break; Break

  IT WAS REPORTED THAT THE CLIP BROKE OFF. UNKNOWN SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17414908 ↗
• MalfunctionFeb 28, 2023Break; Break

  IT WAS REPORTED THAT THE METAL RING BROKE. THERE WAS NO SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16454738 ↗
• MalfunctionFeb 9, 2023Device-Device Incompatibility; Material Deformation; Device-Device Incompatibility; Material Deformation

  IT WAS REPORTED THAT ATTUNE LPS INSERT TRIAL ADAPTER WILL NOT RECEIVE THE INSERTS. POLY TRIALS WILL NOT SLIDE INTO IT CORRECTLY, ONE OF THE FLANGES APPEARS BENT. NOTHING BROKE OFF. NO SURGICAL DELAY WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16338663 ↗
• MalfunctionAug 5, 2022Break; Break

  IT WAS REPORTED THAT THE RETAINING RING BROKE. 1 PIECE WAS BROKEN AND IT WAS REMOVED AND DISCARDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15176648 ↗
• MalfunctionApr 29, 2021Break; Break

  IT WAS REPORTED THAT UPON REMOVAL OF INSERT TRIAL IT WAS NOTICED THAT THE SPRING ON THE METAL TRIAL BROKE. ALL PIECES WERE RETRIEVED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11743814 ↗
• MalfunctionJan 27, 2021Break; Scratched Material; Break; Scratched Material

  TRIAL DAMAGED. NO CONSEQUENCE TO PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11236407 ↗