CLICKLINE 26312Recalls & reported problems
Karl Storz GmbH & Co. KG · CLICKLINE Handle, axial · Class 1
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 6
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 04048551430682), received between Nov 19, 2025 and Feb 24, 2026 — classified as 6 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (5 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
- Failure to Osseointegrate5
- Malposition of Device1
Patient problems
- Failure of Implant6
- Unspecified Infection3
- Osteolysis2
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
InjuryFeb 24, 2026Failure to Osseointegrate
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant; Unspecified Infection
MAUDE report 24434383 ↗InjuryJan 26, 2026Failure to Osseointegrate
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS WITH AN INFECTION.
Patient problems: Failure of Implant; Unspecified Infection
MAUDE report 24185856 ↗InjuryJan 21, 2026Failure to Osseointegrate
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant; Osteolysis
MAUDE report 24129720 ↗InjuryJan 20, 2026Malposition of Device
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT FAILURE. IT WAS STATED THAT THERE WAS NOT ENOUGH BONE ON BUCCAL THE SIDE AFTER PLACEMENT. IT HAD TO BE BUILT UP FIRST.
Patient problems: Failure of Implant
MAUDE report 24115450 ↗InjuryNov 20, 2025Failure to Osseointegrate; Failure to Osseointegrate
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant
MAUDE report 23613038 ↗InjuryNov 19, 2025Failure to Osseointegrate; Failure to Osseointegrate
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant; Osteolysis; Unspecified Infection
MAUDE report 23600770 ↗
Other Hysteroscope accessories devices
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- Olympus A4829OLYMPUS Winter & Ibe GmbH · Hysteroscope Accessories8 reports
- Olympus A4825OLYMPUS Winter & Ibe GmbH · Hysteroscope Accessories8 reports
- n.a. 26153BIKarl Storz GmbH & Co. KG · Hysteroscope accessories3 reports
- OMNI OMNI-G-001Hologic, Inc. · Hysteroscope accessories1 report
- Olympus A4827OLYMPUS Winter & Ibe GmbH · Hysteroscope Accessories1 report
- NA M006550340Boston Scientific Corporation · Hysteroscope accessories1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.