Skip to content

Medline MDS527333SPRecalls & reported problems

Medline Industries, Inc. · LAP,GRASP,ATRAUM,SLIDE LOCK,ROT,5MM,35CM · Class 2

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
4
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10884389959367), received between Sep 10, 2026 and Sep 29, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Break” (2 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.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 4 reportsOct 2026: 0 reports2024202520264
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Break2
  • Corroded1
  • Detachment of Device or Device Component1

Patient problems

  • No Clinical Signs, Symptoms or Conditions4

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

  • OtherSep 29, 2026Break

    It was reported that "TIP OF THE INSTRUMENT ( LAPAROSCOPIC GRASPER ) IS BROKEN."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50933253 ↗
  • MalfunctionSep 21, 2026Break

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50837571 ↗
  • MalfunctionSep 12, 2026Detachment of Device or Device Component

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50746146 ↗
  • MalfunctionSep 10, 2026Corroded

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50716672 ↗

Other LAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES) devices

All LAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES) devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page