LAZIC 35.421Recalls & reported problems
Peter Lazic GmbH · D-CLIP APPLIER/ REMOVER, STANDARD/ MINI, 90 MM WORKING LENGTH, BAYONET, VARIABLE JAW, DOUBLE ACTION, 210 MM · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04250603739630), received between Apr 12, 2024 and Apr 12, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Physical Resistance/Sticking” (1 report).
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
Most reported problems
Device problems
- Physical Resistance/Sticking1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 12, 2024Physical Resistance/Sticking; Physical Resistance/Sticking
OUR CUSTOMER HAS INFORMED US THAT THE APPLIER REMAINS JAMMED. THE APPLIER DOES NOT RELEASE CLIPS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19094762 ↗
Other Applier, Aneurysm Clip devices
- LAZIC 35.411Peter Lazic GmbH · Applier, Aneurysm Clip1 recall1 report
- LAZIC 35.410Peter Lazic GmbH · Applier, Aneurysm Clip1 recall0 reports
- LAZIC 35.412Peter Lazic GmbH · Applier, Aneurysm Clip1 recall0 reports
- AESCULAP FT495TAesculap AG · APPLIER, ANEURYSM CLIP2 reports
- AESCULAP FE908KAesculap AG · APPLIER, ANEURYSM CLIP1 report
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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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