Skip to content

Innomed, Inc. 3645-03Recalls & reported problems

Innomed, Inc. · Suregrip Soft Tissue Grasper 9" · Class 1

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00840277105950), received between Jul 6, 2022 and Jul 6, 2022 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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 18, 2026.

Most reported problems

Device problems

  • Detachment of Device or Device Component2

Patient problems

  • No Clinical Signs, Symptoms or Conditions2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 6, 2022Detachment of Device or Device Component; Detachment of Device or Device Component

    AFTER A CASE, THE SPIKE WAS NOTICED TO BE MISSING FROM THE SUREGRIP SOFT TISSUE GRASPER 9". RAD IMAGING RULED OUT RFB POST CASE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14936774 ↗
  • MalfunctionJul 6, 2022Detachment of Device or Device Component; Detachment of Device or Device Component

    SPD NOTICED THAT THE SUREGRIP TISSUE GRASPER 9" WAS MISSING THE SPIKE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14935174 ↗

Other Pliers, Surgical devices

All Pliers, Surgical devices →

Sources and updates

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