CLICKLINE 33132Recalls & reported problems
Karl Storz GmbH & Co. KG · CLICKLINE Metal Handle · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 04048551125281), received between Mar 12, 2021 and Aug 11, 2026 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Mechanical Problem” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Mechanical Problem3
- Material Separation2
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- Foreign Body In Patient2
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 11, 2026Mechanical Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50202061 ↗MalfunctionAug 11, 2026Mechanical Problem
It was reported that handle snaps/disengages during use. No negative impact in state of health reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50202058 ↗MalfunctionAug 11, 2026Mechanical Problem
It was reported that handle snaps/disengages during use. No negative impact in state of health reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50202051 ↗MalfunctionJan 12, 2023Material Separation; Material Separation
IT WAS REPORTED THAT THERE WAS AN ISSUE WITH THE PRODUCT 33132 HANDLE METAL MANHÈS STYLE RATCHET. ACCORDING TO THE INFORMATION RECEIVED, DURING AN XI ROBOTIC LAP HYSTERECTOMY, ONE SIDE OF THE JAW OF A HUNTER GRASPER BROKE AND THE JAW/BLADE OF THE GRASPER FELL DEEP IN THE ABDOMEN. THE BLADE WAS RECOVERED LAPAROSCOPICALLY. PATIENT HARM IS NOT KNOWN AT DATE OF THIS REPORT. ADDITIONAL INFORMATION HAS BEEN REQUESTED BUT NOT YET RECEIVED AS OF THE DATE OF THIS REPORT AND ADDITIONAL PATIENT INFORMATION IS NOT AVAILABLE.
Patient problems: Foreign Body In Patient
MAUDE report 16146363 ↗MalfunctionMar 12, 2021Material Separation; Material Separation
PER THE MEDWATCH REPORT, DURING A LAPAROSCOPIC APPENDECTOMY, THE TIP OF THE GRASPER BROKE OFF INSIDE THE PATIENT AND WAS RETRIEVED WITH NO HARM TO THE PATIENT. THE PROCEDURE WAS COMPLETED WITH NO OTHER SURGICAL INTERVENTION REQUIRED.
Patient problems: Foreign Body In Patient
MAUDE report 11472970 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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