LAZIC S.35.714Recalls & reported problems
Peter Lazic GmbH · D-Aneurysm MINI Clip TITANIUM permanent, strong curved 4mm · Class 2 · Implant
- 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 04250603731665), received between Apr 9, 2024 and Apr 9, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Wrong Label” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Wrong Label1
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 9, 2024Wrong Label; Wrong Label
OUR CUSTOMER HAS INFORMED US THAT WHEN THE DOCTOR OPENED THE BOX OF S.35.714, THERE WAS A PRODUCT THAT DID NOT MATCH THE CATALOG SPECIFICATIONS. IT SUPPOSED TO BE A STRONG CURVE, BUT THE PRODUCT IN THE BOX HAD A WEAK CURVE. WOULD YOU PLEASE LET US KNOW THE CAUSE OF THE PROBLEM AND MEASURES TP PREVENT FUTURE REOCCURRENCES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19069645 ↗
Other Clip, Aneurysm devices
- LAZIC 45.872Peter Lazic GmbH · Clip, Aneurysm1 recall0 reports
- LAZIC S.45.872Peter Lazic GmbH · Clip, Aneurysm1 recall0 reports
- AESCULAP FE963KAesculap AG · CLIP, ANEURYSM3 reports
- AESCULAP FE964KAesculap AG · CLIP, ANEURYSM3 reports
- AESCULAP FT780DAesculap AG · CLIP, ANEURYSM2 reports
- Medicon 58.60.08Medicon eG. Chirurgiemechaniker-Genossenschaft · CLIP, ANEURYSM2 reports
- AESCULAP FE953KAesculap AG · CLIP, ANEURYSM1 report
- AESCULAP FE962KAesculap AG · CLIP, ANEURYSM1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.