LAZIC S.45.872Recalls & reported problems
Peter Lazic GmbH · L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
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.
Recalls naming this device
- Jul 14, 2023Open, Classified
Wrong product coloring. The paddle clips should be blank, but they are colored blue.
Z-1287-2024 · Root cause: Process control · Recall details · FDA record ↗
Other Clip, Aneurysm devices
- LAZIC 45.872Peter Lazic GmbH · Clip, Aneurysm1 recall0 reports
- AESCULAP FE963KAesculap AG · CLIP, ANEURYSM3 reports
- AESCULAP FE964KAesculap AG · CLIP, ANEURYSM3 reports
- Medicon 58.60.08Medicon eG. Chirurgiemechaniker-Genossenschaft · CLIP, ANEURYSM2 reports
- AESCULAP FT780DAesculap AG · CLIP, ANEURYSM2 reports
- AESCULAP FT599TAesculap AG · CLIP, ANEURYSM1 report
- LAZIC S.35.714Peter Lazic GmbH · Clip, Aneurysm1 report
- AESCULAP FE953KAesculap AG · CLIP, ANEURYSM1 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
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- 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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