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LAZIC 35.412Recalls & reported problems

Peter Lazic GmbH · D-CLIP APPLIER/ REMOVER, STANDARD/ MINI, 110 MM WORKING LENGTH, BAYONET, RIGID JAW, DOUBLE ACTION, 230 MM · Class 2

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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. 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-1279-2024 · Root cause: Device Design · FDA record ↗

Other Applier, Aneurysm Clip devices

All Applier, Aneurysm Clip devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.