FDAFDA · Food and drugs·Recall number Z-1278-2024
D-Clip Standard/Mini Applier, 210mm bayonet, jaw rigid, double action.
Published March 20, 2024 · Recall initiated: October 6, 2023
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Peter Lazic Gmbh
- Distributor
- US Nationwide distribution in the state of ME.
- Lot
- Model number: 35.411; UDI/DI: 04250603739609; All Lot numbers.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- Germany
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