LPS 2987-70-001Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10603295158790), received between Jul 28, 2022 and Nov 17, 2023 — classified as 5 malfunctions.

The most frequently reported specific device problem is “Failure to Cut” (3 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 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 17, 2023Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED THAT CALCAR REAMER WOULDN'T HOLD THE PILOT SHAFTS AND IT KEPT FALLING OFF.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18160089 ↗
• MalfunctionAug 11, 2023Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED THAT THE LPS CALCAR PLANER SMALL AND THE LPS BEVEL REAMER INSERT SZ 13 WERE STUCK TOGETHER AND WON'T COME APART. THE V-TAMP IS SLIGHTLY DAMAGED FROM BEING USED. NO SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17511750 ↗
• MalfunctionJul 10, 2023Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT CALCAR PLANERS ARE DULL.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17289636 ↗
• MalfunctionJul 10, 2023Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT CALCAR PLANERS ARE DULL.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17289634 ↗
• MalfunctionJul 28, 2022Failure to Cut; Failure to Cut

  IT WAS REPORTED THAT THE CALCAR REAMER WAS DULL.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15126065 ↗