Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
D-Clip Standard/Mini Applier Recalled by Peter Lazic Gmbh Due to Customer complaint received that reported the applier failed...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Peter Lazic Gmbh directly.
Affected Products
D-Clip Standard/Mini Applier, 230mm bayonet, jaw rigid, double action.
Quantity: 10 units
Why Was This 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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Peter Lazic Gmbh
Peter Lazic Gmbh has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report