Legion 71441979Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885556536988), received between Mar 14, 2021 and Mar 14, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Reprocessing Problem” (1 report).

2 other recalls cover devices cleared under the same FDA submission (K162775); they may or may not involve this specific model.

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

• MalfunctionMar 14, 2021Device Reprocessing Problem; Device Reprocessing Problem

  IT WAS REPORTED THAT THE HOLES ON THE INNER TUBE WHERE CONE HANDLE SLIDES IN ARE FILLED WITH DEBRIS THAT SPD CANNOT CLEAN OUT. NO CASE INVOLVED, FOUND DURING INSPECTION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11478849 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K162775. One submission often covers many models, so check the product and lot details in each record.

• Z-2624-2017 · May 30, 2017 · Terminated
  LEGION(R) FEM CONE IMPACTOR HEADS: a) REF 71441976, ID 18MM b) REF 71441977, ID 20MM c) REF 71441978, ID 22MM
• Z-2625-2017 · May 30, 2017 · Terminated
  LEGION(R) TIB CONE IMPACTOR HEADS: a) REF 71441972, ID 24MM b) REF 71441971, ID 22MM c) REF 71441973, ID 26MM d) REF 71441974, ID 28MM e) REF 71441975, ID 30MM