Peter Lazic Gmbh recalls D-Clip Standard/Mini Applier, 230mm bayonet, jaw rigid, double action.
- Recall date
- October 6, 2023
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1279-2024
- FDA classification
- Class II
- Brand / firm
- Peter Lazic Gmbh
- Sold / distributed
- US Nationwide distribution in the state of ME.
Why it was recalled
Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
D-Clip Standard/Mini Applier, 230mm bayonet, jaw rigid, double action.
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