LAZIC 35.410Recalls & reported problems
Peter Lazic GmbH · D-CLIP APPLIER STANDARD/ MINI, 70 MM WORKING LENGTH, BAYONET, RIGID JAW, DOUBLE ACTION, 190 MM · Class 2
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
- Oct 6, 2023Open, Classified
Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.
Z-1277-2024 · Root cause: Device Design · Recall details · FDA record ↗
Other Applier, Aneurysm Clip devices
- LAZIC 35.411Peter Lazic GmbH · Applier, Aneurysm Clip1 recall1 report
- LAZIC 35.412Peter Lazic GmbH · Applier, Aneurysm Clip1 recall0 reports
- AESCULAP FT495TAesculap AG · APPLIER, ANEURYSM CLIP2 reports
- LAZIC 35.421Peter Lazic GmbH · Applier, Aneurysm Clip1 report
- 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
- 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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